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FDA 510(k)

C-QUR LITE MESH V-PATCH

K-Number: K080688 · 2008-04-16

Decision Date2008-04-16
Product CodeFTL
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

C-QUR LITE MESH V-PATCH is the device name listed in this FDA 510(k) record. The listed applicant is Atrium Medical Corp.. It received FDA 510(k) clearance on 2008-04-16 under 510(k) number K080688. The device is classified under product code FTL. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the C-QUR LITE MESH V-PATCH?

C-QUR LITE MESH V-PATCH is a medical device that received FDA 510(k) clearance on 2008-04-16. The listed applicant is Atrium Medical Corp.. The 510(k) number is K080688.

When did C-QUR LITE MESH V-PATCH receive FDA 510(k) clearance?

C-QUR LITE MESH V-PATCH received FDA 510(k) clearance on 2008-04-16, under 510(k) number K080688.

Who is the listed applicant for C-QUR LITE MESH V-PATCH?

The FDA 510(k) record lists Atrium Medical Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for C-QUR LITE MESH V-PATCH?

The FDA product code for C-QUR LITE MESH V-PATCH is FTL.

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 Atrium Medical Corp. 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 63 devices →

Related Devices (Code: FTL)

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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