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FDA 510(k)

CARRINGTON WOUND DRESSING 4X4(TM)

K-Number: K915001 · 1992-01-31

ApplicantCarrington Laboratories, Inc.
Decision Date1992-01-31
Product CodeMGQ
DecisionSubstantially Equivalent

Device Summary

CARRINGTON WOUND DRESSING 4X4(TM) is the device name listed in this FDA 510(k) record. The listed applicant is Carrington Laboratories, Inc.. It received FDA 510(k) clearance on 1992-01-31 under 510(k) number K915001. The device is classified under product code MGQ. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CARRINGTON WOUND DRESSING 4X4(TM)?

CARRINGTON WOUND DRESSING 4X4(TM) is a medical device that received FDA 510(k) clearance on 1992-01-31. The listed applicant is Carrington Laboratories, Inc.. The 510(k) number is K915001.

When did CARRINGTON WOUND DRESSING 4X4(TM) receive FDA 510(k) clearance?

CARRINGTON WOUND DRESSING 4X4(TM) received FDA 510(k) clearance on 1992-01-31, under 510(k) number K915001.

Who is the listed applicant for CARRINGTON WOUND DRESSING 4X4(TM)?

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

What is the FDA product code for CARRINGTON WOUND DRESSING 4X4(TM)?

The FDA product code for CARRINGTON WOUND DRESSING 4X4(TM) is MGQ.

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Other records listing Carrington Laboratories, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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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