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FDA 510(k)

AQUACEL AG SURGICAL

K-Number: K091034 · 2009-12-16

ApplicantConvatec
Decision Date2009-12-16
Product CodeFRO
DecisionSubstantially Equivalent

Device Summary

AQUACEL AG SURGICAL is the device name listed in this FDA 510(k) record. The listed applicant is Convatec. It received FDA 510(k) clearance on 2009-12-16 under 510(k) number K091034. The device is classified under product code FRO. Product code FRO falls under the category of Anesthesiology, which includes devices for anesthetic delivery and patient monitoring. Devices in this category are subject to specific FDA regulatory requirements. FDA Decision: Substantially Equivalent.

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.

View all 8 devices →

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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