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FDA 510(k)

BRADY MEDICAL PRODUCTS HYSORB(TM) WOUND DRESSING

K-Number: K936052 · 1994-03-07

Decision Date1994-03-07
Product CodeKMF
Advisory CommitteeHO
DecisionSubstantially Equivalent for Some Indications

Device Summary

BRADY MEDICAL PRODUCTS HYSORB(TM) 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 1994-03-07 under 510(k) number K936052. The device is classified under product code KMF. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent for Some Indications.

Frequently Asked Questions

What is the BRADY MEDICAL PRODUCTS HYSORB(TM) WOUND DRESSING?

BRADY MEDICAL PRODUCTS HYSORB(TM) WOUND DRESSING is a medical device that received FDA 510(k) clearance on 1994-03-07. The listed applicant is Brady Medical Products Co.. The 510(k) number is K936052.

When did BRADY MEDICAL PRODUCTS HYSORB(TM) WOUND DRESSING receive FDA 510(k) clearance?

BRADY MEDICAL PRODUCTS HYSORB(TM) WOUND DRESSING received FDA 510(k) clearance on 1994-03-07, under 510(k) number K936052.

Who is the listed applicant for BRADY MEDICAL PRODUCTS HYSORB(TM) 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 BRADY MEDICAL PRODUCTS HYSORB(TM) WOUND DRESSING?

The FDA product code for BRADY MEDICAL PRODUCTS HYSORB(TM) WOUND DRESSING is KMF.

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: KMF)

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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