BIOFILM TRANS. ISLAND, ISLAND ULCER & WOUND DRESS.
K-Number: K872099 · 1987-06-30
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Device Summary
Frequently Asked Questions
What is the BIOFILM TRANS. ISLAND, ISLAND ULCER & WOUND DRESS.?
BIOFILM TRANS. ISLAND, ISLAND ULCER & WOUND DRESS. 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 K872099.
When did BIOFILM TRANS. ISLAND, ISLAND ULCER & WOUND DRESS. receive FDA 510(k) clearance?
BIOFILM TRANS. ISLAND, ISLAND ULCER & WOUND DRESS. received FDA 510(k) clearance on 1987-06-30, under 510(k) number K872099.
Who is the listed applicant for BIOFILM TRANS. ISLAND, ISLAND ULCER & WOUND DRESS.?
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 TRANS. ISLAND, ISLAND ULCER & WOUND DRESS.?
The FDA product code for BIOFILM TRANS. ISLAND, ISLAND ULCER & WOUND DRESS. 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
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
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