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FDA 510(k)

CATO FIRST PICC KIT

K-Number: K945499 · 1995-02-07

ApplicantCatco Medical, Inc.
Decision Date1995-02-07
Product CodeLJS
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

CATO FIRST PICC KIT is the device name listed in this FDA 510(k) record. The listed applicant is Catco Medical, Inc.. It received FDA 510(k) clearance on 1995-02-07 under 510(k) number K945499. 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 CATO FIRST PICC KIT?

CATO FIRST PICC KIT is a medical device that received FDA 510(k) clearance on 1995-02-07. The listed applicant is Catco Medical, Inc.. The 510(k) number is K945499.

When did CATO FIRST PICC KIT receive FDA 510(k) clearance?

CATO FIRST PICC KIT received FDA 510(k) clearance on 1995-02-07, under 510(k) number K945499.

Who is the listed applicant for CATO FIRST PICC KIT?

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

What is the FDA product code for CATO FIRST PICC KIT?

The FDA product code for CATO FIRST PICC KIT is LJS.

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Other records listing Catco Medical, Inc. 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.

K945728CATCO THORACIC CATHETERK944368CATCO SILICONE UMBILICAL VESSEL CATHETERK944410CATCO SILICONE DUAL LUMEN UMBILICAL VESSEL CATHETERK944336CATCO UMBILICAL VESSEL CATHETERK944367CATCO POLYURETHANE UMBILICAL VESSEL CATHETERK944685CATO FIRST PICC-DUAL LUMEN

View all 12 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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