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FDA 510(k)

MEDCOMP P-CATH

K-Number: K953811 · 1996-07-25

ApplicantMedcomp
Decision Date1996-07-25
Product CodeFOZ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

MEDCOMP P-CATH is the device name listed in this FDA 510(k) record. The listed applicant is Medcomp. It received FDA 510(k) clearance on 1996-07-25 under 510(k) number K953811. The device is classified under product code FOZ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDCOMP P-CATH?

MEDCOMP P-CATH is a medical device that received FDA 510(k) clearance on 1996-07-25. The listed applicant is Medcomp. The 510(k) number is K953811.

When did MEDCOMP P-CATH receive FDA 510(k) clearance?

MEDCOMP P-CATH received FDA 510(k) clearance on 1996-07-25, under 510(k) number K953811.

Who is the listed applicant for MEDCOMP P-CATH?

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

What is the FDA product code for MEDCOMP P-CATH?

The FDA product code for MEDCOMP P-CATH is FOZ.

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Other records listing Medcomp 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.

K123292T3K1029662.6F X 20CM VASCU-PICC, 2.6F X 50CM VASCU-PICCK091954MICRO-STICK SETK092347PRO-PICC CTK091953PRO-PICCK090394VALVED TEARWAY INTRODUCER

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Related Devices (Code: FOZ)

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.

K260432Ruby Intravascular CatheterVenocare, Inc.K260165Unimpregnated Central Venous CatheterSpectrum VascularK261041ClearSafe Closed SystemMedSource Labs, LLCK260539MedSource QuickSafe™ Safety IV Catheter; MedSource PurSafe™ Safety IV CatheterMedSource Labs, LLCK253235Introcan Safety® Deep Access XL IV CatheterB.Braun Medical, Inc.K252137BD Insyte™ IV CatheterBecton Dickinson Infusion Therapy Systems, 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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