AQUACEL AG SURGICAL
K-Number: K091034 · 2009-12-16
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Device Summary
Frequently Asked Questions
What is the AQUACEL AG SURGICAL?
AQUACEL AG SURGICAL is a medical device that received FDA 510(k) clearance on 2009-12-16. The listed applicant is Convatec. The 510(k) number is K091034.
When did AQUACEL AG SURGICAL receive FDA 510(k) clearance?
AQUACEL AG SURGICAL received FDA 510(k) clearance on 2009-12-16, under 510(k) number K091034.
Who is the listed applicant for AQUACEL AG SURGICAL?
The FDA 510(k) record lists Convatec as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for AQUACEL AG SURGICAL?
The FDA product code for AQUACEL AG SURGICAL 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 Convatec 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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