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FDA 510(k)

QUEGEL HYDROPHILIC WOUND DRESSING

K-Number: K955400 · 1996-02-09

Decision Date1996-02-09
Product CodeMGQ
DecisionSubstantially Equivalent for Some Indications

Device Summary

QUEGEL HYDROPHILIC WOUND DRESSING is the device name listed in this FDA 510(k) record. The listed applicant is Questor Pharma, Inc.. It received FDA 510(k) clearance on 1996-02-09 under 510(k) number K955400. The device is classified under product code MGQ. FDA Decision: Substantially Equivalent for Some Indications.

Frequently Asked Questions

What is the QUEGEL HYDROPHILIC WOUND DRESSING?

QUEGEL HYDROPHILIC WOUND DRESSING is a medical device that received FDA 510(k) clearance on 1996-02-09. The listed applicant is Questor Pharma, Inc.. The 510(k) number is K955400.

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

QUEGEL HYDROPHILIC WOUND DRESSING received FDA 510(k) clearance on 1996-02-09, under 510(k) number K955400.

Who is the listed applicant for QUEGEL HYDROPHILIC WOUND DRESSING?

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

What is the FDA product code for QUEGEL HYDROPHILIC WOUND DRESSING?

The FDA product code for QUEGEL HYDROPHILIC WOUND DRESSING is MGQ.

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.

Related Devices (Code: MGQ)

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.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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