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FDA 510(k)

BIOLEX IMPREGNATED WOUND DRESSING

K-Number: K935096 · 1994-02-17

ApplicantC.R. Bard, Inc.
Decision Date1994-02-17
Product CodeMGQ
DecisionSubstantially Equivalent

Device Summary

BIOLEX IMPREGNATED WOUND DRESSING 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 1994-02-17 under 510(k) number K935096. The device is classified under product code MGQ. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BIOLEX IMPREGNATED WOUND DRESSING?

BIOLEX IMPREGNATED WOUND DRESSING is a medical device that received FDA 510(k) clearance on 1994-02-17. The listed applicant is C.R. Bard, Inc.. The 510(k) number is K935096.

When did BIOLEX IMPREGNATED WOUND DRESSING receive FDA 510(k) clearance?

BIOLEX IMPREGNATED WOUND DRESSING received FDA 510(k) clearance on 1994-02-17, under 510(k) number K935096.

Who is the listed applicant for BIOLEX IMPREGNATED WOUND DRESSING?

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 BIOLEX IMPREGNATED WOUND DRESSING?

The FDA product code for BIOLEX IMPREGNATED WOUND DRESSING is MGQ.

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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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