FDA 510(k)

BARD VENTRALEX HERNIA PATCH, MODELS 0010302, 0010301

K-Number: K021736 · 2002-07-16

Decision Date2002-07-16

Product CodeFTL

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

BARD VENTRALEX HERNIA PATCH, MODELS 0010302, 0010301 is the device name listed in this FDA 510(k) record. The listed applicant is C.R. Bard, Inc.. It received FDA 510(k) clearance on 2002-07-16 under 510(k) number K021736. The device is classified under product code FTL. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BARD VENTRALEX HERNIA PATCH, MODELS 0010302, 0010301?

BARD VENTRALEX HERNIA PATCH, MODELS 0010302, 0010301 is a medical device that received FDA 510(k) clearance on 2002-07-16. The listed applicant is C.R. Bard, Inc.. The 510(k) number is K021736.

When did BARD VENTRALEX HERNIA PATCH, MODELS 0010302, 0010301 receive FDA 510(k) clearance?

BARD VENTRALEX HERNIA PATCH, MODELS 0010302, 0010301 received FDA 510(k) clearance on 2002-07-16, under 510(k) number K021736.

Who is the listed applicant for BARD VENTRALEX HERNIA PATCH, MODELS 0010302, 0010301?

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

What is the FDA product code for BARD VENTRALEX HERNIA PATCH, MODELS 0010302, 0010301?

The FDA product code for BARD VENTRALEX HERNIA PATCH, MODELS 0010302, 0010301 is FTL.

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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.