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FDA 510(k)

DEROYAL WOUND DRESSING

K-Number: K912472 · 1991-10-02

Decision Date1991-10-02
Product CodeMGO
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

DEROYAL WOUND DRESSING is the device name listed in this FDA 510(k) record. The listed applicant is Deroyal Industries, Inc.. It received FDA 510(k) clearance on 1991-10-02 under 510(k) number K912472. The device is classified under product code MGO. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DEROYAL WOUND DRESSING?

DEROYAL WOUND DRESSING is a medical device that received FDA 510(k) clearance on 1991-10-02. The listed applicant is Deroyal Industries, Inc.. The 510(k) number is K912472.

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

DEROYAL WOUND DRESSING received FDA 510(k) clearance on 1991-10-02, under 510(k) number K912472.

Who is the listed applicant for DEROYAL WOUND DRESSING?

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

What is the FDA product code for DEROYAL WOUND DRESSING?

The FDA product code for DEROYAL WOUND DRESSING is MGO.

Related Clinical Trials

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.

Other records listing Deroyal Industries, 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

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