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FDA 510(k)

V-CATH DUAL LUMEN E.S.P. PERIPHERAL INSERTED CENTRAL CATHETER

K-Number: K953300 · 1996-04-30

ApplicantHdc Corp.
Decision Date1996-04-30
Product CodeLJS
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

V-CATH DUAL LUMEN E.S.P. PERIPHERAL INSERTED CENTRAL CATHETER is the device name listed in this FDA 510(k) record. The listed applicant is Hdc Corp.. It received FDA 510(k) clearance on 1996-04-30 under 510(k) number K953300. The device is classified under product code LJS. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the V-CATH DUAL LUMEN E.S.P. PERIPHERAL INSERTED CENTRAL CATHETER?

V-CATH DUAL LUMEN E.S.P. PERIPHERAL INSERTED CENTRAL CATHETER is a medical device that received FDA 510(k) clearance on 1996-04-30. The listed applicant is Hdc Corp.. The 510(k) number is K953300.

When did V-CATH DUAL LUMEN E.S.P. PERIPHERAL INSERTED CENTRAL CATHETER receive FDA 510(k) clearance?

V-CATH DUAL LUMEN E.S.P. PERIPHERAL INSERTED CENTRAL CATHETER received FDA 510(k) clearance on 1996-04-30, under 510(k) number K953300.

Who is the listed applicant for V-CATH DUAL LUMEN E.S.P. PERIPHERAL INSERTED CENTRAL CATHETER?

The FDA 510(k) record lists Hdc Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for V-CATH DUAL LUMEN E.S.P. PERIPHERAL INSERTED CENTRAL CATHETER?

The FDA product code for V-CATH DUAL LUMEN E.S.P. PERIPHERAL INSERTED CENTRAL CATHETER is LJS.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Hdc Corp. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K071875V-CATH POLY PICCK023342NEURO-TRACE III KIT, NEURO-TRACE III REGIONAL BLOCK CABLE, NEURO-TRACE III NERVE MAPPING PROBE, NEURO-TRACE III NERVE BGK033853MODIFICATION TO V-CATH POLY PICCK032404SELDINGER SAFETY NEEDLE INTRODUCERK022752PANDIN CONTINUOUS NERVE STIMULATING CATHETER, MODELS 561-18-05, 561-18-09, 561-18-15, 562-18-05, 562-18-09 & 562-18-15K022099SAFE-T-PEEL SAFETY NEEDLE/INTRODUCER, MODELS 350-300 S, 360-300'S,380-300'S,390-300'S

View all 30 devices →

Related Devices (Code: LJS)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K260929Neonav ECG Tip Location SystemNavi Medical TechnologiesK252373BioFlo Hybrid PICC with ENDEXO Technology and PASV Valve Technology; BioFlo PICC with ENDEXO Technology and PASV Valve Technology; BioFlo PICC with ENDEXO Technology; BioFlo Midline Catheter; Xcela Power Injectable PICC; Xcela PICC with PASV Valve Technology; Xcela Hybrid PICC with PASV Valve TechnologySpectrum VascularK252792PM2™ System with ECGuide™ ConnectorPiccolo Medical, Inc.K243458HydroPICC 4Fr Single Lumen Marked catheter, 130 cm guidewire - Basic Kit (70001301); HydroPICC 4Fr Single Lumen Marked catheter, 70 cm guidewire - Basic Kit (70001302); HydroPICC 4Fr Single Lumen Marked catheter - Maximal Barrier kit (70001304); HydroPICC 5Fr Dual Lumen Marked catheter, 130 cm guidewire - Basic Kit (70002301); HydroPICC 5Fr Dual Lumen Marked catheter, 70 cm guidewire - Basic Kit (70002302); HydroPICC 5Fr Dual Lumen Marked catheter - Maximal Barrier kit (70002304); HydrAccess Vascular, Inc.K251212Dual Lumen 5Fr HydroPICC Catheter (PICC-251CM) (PICC-251CM); Dual Lumen 5Fr HydroPICC Catheter (PICC-252CM) (PICC-252CM)Access Vascular, Inc.K243484PM2+ System and SmartPICC StyletPiccolo Medical, Inc.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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