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FDA 510(k)

TRANSORB(TM) ULCER & WOUND DRESSING

K-Number: K922666 · 1992-11-23

Decision Date1992-11-23
Product CodeNAE
Advisory CommitteeSU
DecisionSubstantially Equivalent for Some Indications

Device Summary

TRANSORB(TM) ULCER & WOUND DRESSING is the device name listed in this FDA 510(k) record. The listed applicant is Brady Medical Products Co.. It received FDA 510(k) clearance on 1992-11-23 under 510(k) number K922666. The device is classified under product code NAE. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent for Some Indications.

Frequently Asked Questions

What is the TRANSORB(TM) ULCER & WOUND DRESSING?

TRANSORB(TM) ULCER & WOUND DRESSING is a medical device that received FDA 510(k) clearance on 1992-11-23. The listed applicant is Brady Medical Products Co.. The 510(k) number is K922666.

When did TRANSORB(TM) ULCER & WOUND DRESSING receive FDA 510(k) clearance?

TRANSORB(TM) ULCER & WOUND DRESSING received FDA 510(k) clearance on 1992-11-23, under 510(k) number K922666.

Who is the listed applicant for TRANSORB(TM) ULCER & WOUND DRESSING?

The FDA 510(k) record lists Brady Medical Products Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TRANSORB(TM) ULCER & WOUND DRESSING?

The FDA product code for TRANSORB(TM) ULCER & WOUND DRESSING is NAE.

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 Brady Medical Products Co. 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.

Related Devices (Code: NAE)

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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