TRIOSYN T40 ANTIMICROBIAL WOUND DRESSING
K-Number: K051542 · 2006-03-17
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Device Summary
Frequently Asked Questions
What is the TRIOSYN T40 ANTIMICROBIAL WOUND DRESSING?
TRIOSYN T40 ANTIMICROBIAL WOUND DRESSING is a medical device that received FDA 510(k) clearance on 2006-03-17. The listed applicant is Triosyn Corp.. The 510(k) number is K051542.
When did TRIOSYN T40 ANTIMICROBIAL WOUND DRESSING receive FDA 510(k) clearance?
TRIOSYN T40 ANTIMICROBIAL WOUND DRESSING received FDA 510(k) clearance on 2006-03-17, under 510(k) number K051542.
Who is the listed applicant for TRIOSYN T40 ANTIMICROBIAL WOUND DRESSING?
The FDA 510(k) record lists Triosyn Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for TRIOSYN T40 ANTIMICROBIAL WOUND DRESSING?
The FDA product code for TRIOSYN T40 ANTIMICROBIAL WOUND DRESSING is FRO. This falls under the Anesthesiology category.
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.
Related Devices (Code: FRO)
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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