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FDA 510(k)

BIOFILM TRANSORBENT ULCER AND WOUND DRESSING

K-Number: K872100 · 1987-06-30

Decision Date1987-06-30
Product CodeNAD
Advisory CommitteeSU
DecisionSubstantially Equivalent for Some Indications

Device Summary

BIOFILM TRANSORBENT ULCER AND WOUND DRESSING is the device name listed in this FDA 510(k) record. The listed applicant is The Bfgoodrich Co.. It received FDA 510(k) clearance on 1987-06-30 under 510(k) number K872100. The device is classified under product code NAD. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent for Some Indications.

Frequently Asked Questions

What is the BIOFILM TRANSORBENT ULCER AND WOUND DRESSING?

BIOFILM TRANSORBENT ULCER AND WOUND DRESSING is a medical device that received FDA 510(k) clearance on 1987-06-30. The listed applicant is The Bfgoodrich Co.. The 510(k) number is K872100.

When did BIOFILM TRANSORBENT ULCER AND WOUND DRESSING receive FDA 510(k) clearance?

BIOFILM TRANSORBENT ULCER AND WOUND DRESSING received FDA 510(k) clearance on 1987-06-30, under 510(k) number K872100.

Who is the listed applicant for BIOFILM TRANSORBENT ULCER AND WOUND DRESSING?

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

What is the FDA product code for BIOFILM TRANSORBENT ULCER AND WOUND DRESSING?

The FDA product code for BIOFILM TRANSORBENT ULCER AND WOUND DRESSING is NAD.

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 The Bfgoodrich 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: NAD)

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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