FDA 510(k)

DUAL LUMEN PERIPHERALLY INSERTED VENOUS CATHETER

K-Number: K932430 · 1994-05-02

Decision Date1994-05-02

Product CodeLJS

Advisory CommitteeHO

DecisionUnknown

Device Summary

DUAL LUMEN PERIPHERALLY INSERTED VENOUS CATHETER is the device name listed in this FDA 510(k) record. The listed applicant is Pharmacia Deltec, Inc.. It received FDA 510(k) clearance on 1994-05-02 under 510(k) number K932430. The device is classified under product code LJS. It was reviewed by the HO advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the DUAL LUMEN PERIPHERALLY INSERTED VENOUS CATHETER?

DUAL LUMEN PERIPHERALLY INSERTED VENOUS CATHETER is a medical device that received FDA 510(k) clearance on 1994-05-02. The listed applicant is Pharmacia Deltec, Inc.. The 510(k) number is K932430.

When did DUAL LUMEN PERIPHERALLY INSERTED VENOUS CATHETER receive FDA 510(k) clearance?

DUAL LUMEN PERIPHERALLY INSERTED VENOUS CATHETER received FDA 510(k) clearance on 1994-05-02, under 510(k) number K932430.

Who is the listed applicant for DUAL LUMEN PERIPHERALLY INSERTED VENOUS CATHETER?

The FDA 510(k) record lists Pharmacia Deltec, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DUAL LUMEN PERIPHERALLY INSERTED VENOUS CATHETER?

The FDA product code for DUAL LUMEN PERIPHERALLY INSERTED VENOUS 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_RECRUITING NCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITING NCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDED NCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Pharmacia Deltec, Inc. as applicant

K943310MODEL 6100 AMBULATORY INFUSION SYSTEM K942046PHARMACIA DELTEC EXTENSION SET WITH ANTI-SIPHON VALVE K942161LOCKBOX K942024PORT-A-CATH LOW PROFILE IMPLANTABLE VENOUS ACCESS SYSTEM K941445EXTENSION SET WITH ANTI-SIPHON VALVE K931073CATH-FINDER

View all 43 devices →

Related Devices (Code: LJS)

K260929Neonav ECG Tip Location SystemNavi Medical Technologies K252373BioFlo 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 Vascular K252792PM2™ 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.