FDA 510(k)

VYGON PREMI-CATH - LONG TERM CATHETER

K-Number: K954302 · 1996-06-17

Decision Date1996-06-17

Product CodeLJS

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

VYGON PREMI-CATH - LONG TERM CATHETER is the device name listed in this FDA 510(k) record. The listed applicant is Vygon Corp.. It received FDA 510(k) clearance on 1996-06-17 under 510(k) number K954302. 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 VYGON PREMI-CATH - LONG TERM CATHETER?

VYGON PREMI-CATH - LONG TERM CATHETER is a medical device that received FDA 510(k) clearance on 1996-06-17. The listed applicant is Vygon Corp.. The 510(k) number is K954302.

When did VYGON PREMI-CATH - LONG TERM CATHETER receive FDA 510(k) clearance?

VYGON PREMI-CATH - LONG TERM CATHETER received FDA 510(k) clearance on 1996-06-17, under 510(k) number K954302.

Who is the listed applicant for VYGON PREMI-CATH - LONG TERM CATHETER?

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

What is the FDA product code for VYGON PREMI-CATH - LONG TERM CATHETER?

The FDA product code for VYGON PREMI-CATH - LONG TERM CATHETER is LJS.

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Related Devices (Code: LJS)

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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.