STERIL-DERM TRANSPARENT WOUND DRESSING
K-Number: K892837 · 1989-08-01
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Device Summary
Frequently Asked Questions
What is the STERIL-DERM TRANSPARENT WOUND DRESSING?
STERIL-DERM TRANSPARENT WOUND DRESSING is a medical device that received FDA 510(k) clearance on 1989-08-01. The listed applicant is Biointerface Technologies, Inc.. The 510(k) number is K892837.
When did STERIL-DERM TRANSPARENT WOUND DRESSING receive FDA 510(k) clearance?
STERIL-DERM TRANSPARENT WOUND DRESSING received FDA 510(k) clearance on 1989-08-01, under 510(k) number K892837.
Who is the listed applicant for STERIL-DERM TRANSPARENT WOUND DRESSING?
The FDA 510(k) record lists Biointerface Technologies, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for STERIL-DERM TRANSPARENT WOUND DRESSING?
The FDA product code for STERIL-DERM TRANSPARENT 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 Biointerface Technologies, Inc. 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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