FDA 510(k)

FOOTPRINT MEDICAL PERIPHERALLY INSERTED CENTRAL CATHETER

K-Number: K093252 · 2009-12-17

Decision Date2009-12-17

Product CodeLJS

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

FOOTPRINT MEDICAL PERIPHERALLY INSERTED CENTRAL CATHETER is the device name listed in this FDA 510(k) record. The listed applicant is Footprint Medical, Inc.. It received FDA 510(k) clearance on 2009-12-17 under 510(k) number K093252. 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 FOOTPRINT MEDICAL PERIPHERALLY INSERTED CENTRAL CATHETER?

FOOTPRINT MEDICAL PERIPHERALLY INSERTED CENTRAL CATHETER is a medical device that received FDA 510(k) clearance on 2009-12-17. The listed applicant is Footprint Medical, Inc.. The 510(k) number is K093252.

When did FOOTPRINT MEDICAL PERIPHERALLY INSERTED CENTRAL CATHETER receive FDA 510(k) clearance?

FOOTPRINT MEDICAL PERIPHERALLY INSERTED CENTRAL CATHETER received FDA 510(k) clearance on 2009-12-17, under 510(k) number K093252.

Who is the listed applicant for FOOTPRINT MEDICAL PERIPHERALLY INSERTED CENTRAL CATHETER?

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

What is the FDA product code for FOOTPRINT MEDICAL PERIPHERALLY INSERTED CENTRAL CATHETER?

The FDA product code for FOOTPRINT MEDICAL PERIPHERALLY INSERTED CENTRAL CATHETER is LJS.

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Other records listing Footprint Medical, Inc. as applicant

K130507FOOTPRINT MEDICAL POLYURETHANE PICC CATHETER K120304FOOTPRINT MEDICAL POLYURETHANE UMBILICAL CATHETER K102548FOOTPRINT MEDICAL POLYURETHANE FEEDING TUBE

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

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