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FDA 510(k)

BARD MARLEX MESH DART

K-Number: K922916 · 1992-08-24

ApplicantC.R. Bard, Inc.
Decision Date1992-08-24
Product CodeFTL
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

BARD MARLEX MESH DART 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 1992-08-24 under 510(k) number K922916. 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 MARLEX MESH DART?

BARD MARLEX MESH DART is a medical device that received FDA 510(k) clearance on 1992-08-24. The listed applicant is C.R. Bard, Inc.. The 510(k) number is K922916.

When did BARD MARLEX MESH DART receive FDA 510(k) clearance?

BARD MARLEX MESH DART received FDA 510(k) clearance on 1992-08-24, under 510(k) number K922916.

Who is the listed applicant for BARD MARLEX MESH DART?

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 MARLEX MESH DART?

The FDA product code for BARD MARLEX MESH DART 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.

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