FDA 510(k)

SMALL BARD VENTRALEX PATCH

K-Number: K024008 · 2003-02-20

Decision Date2003-02-20

Product CodeFTL

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

SMALL BARD VENTRALEX PATCH 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 2003-02-20 under 510(k) number K024008. 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 SMALL BARD VENTRALEX PATCH?

SMALL BARD VENTRALEX PATCH is a medical device that received FDA 510(k) clearance on 2003-02-20. The listed applicant is C.R. Bard, Inc.. The 510(k) number is K024008.

When did SMALL BARD VENTRALEX PATCH receive FDA 510(k) clearance?

SMALL BARD VENTRALEX PATCH received FDA 510(k) clearance on 2003-02-20, under 510(k) number K024008.

Who is the listed applicant for SMALL BARD VENTRALEX PATCH?

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 SMALL BARD VENTRALEX PATCH?

The FDA product code for SMALL BARD VENTRALEX PATCH is FTL.

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Related Devices (Code: FTL)

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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.