SILVER ANTIMICROBIAL WOUND GEL
K-Number: K073197 · 2008-08-28
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Device Summary
Frequently Asked Questions
What is the SILVER ANTIMICROBIAL WOUND GEL?
SILVER ANTIMICROBIAL WOUND GEL is a medical device that received FDA 510(k) clearance on 2008-08-28. The listed applicant is Advanced Medical Solutions Limited. The 510(k) number is K073197.
When did SILVER ANTIMICROBIAL WOUND GEL receive FDA 510(k) clearance?
SILVER ANTIMICROBIAL WOUND GEL received FDA 510(k) clearance on 2008-08-28, under 510(k) number K073197.
Who is the listed applicant for SILVER ANTIMICROBIAL WOUND GEL?
The FDA 510(k) record lists Advanced Medical Solutions Limited as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SILVER ANTIMICROBIAL WOUND GEL?
The FDA product code for SILVER ANTIMICROBIAL WOUND GEL 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.
Other records listing Advanced Medical Solutions Limited 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: 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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