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FDA 510(k)

ATRICLIP GILLINOV-COSGROVE LAA CLIP

K-Number: K131107 · 2013-05-14

ApplicantAtriCure, Inc.
Decision Date2013-05-14
Product CodeFZP
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

ATRICLIP GILLINOV-COSGROVE LAA CLIP is the device name listed in this FDA 510(k) record. The listed applicant is AtriCure, Inc.. It received FDA 510(k) clearance on 2013-05-14 under 510(k) number K131107. The device is classified under product code FZP. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ATRICLIP GILLINOV-COSGROVE LAA CLIP?

ATRICLIP GILLINOV-COSGROVE LAA CLIP is a medical device that received FDA 510(k) clearance on 2013-05-14. The listed applicant is AtriCure, Inc.. The 510(k) number is K131107.

When did ATRICLIP GILLINOV-COSGROVE LAA CLIP receive FDA 510(k) clearance?

ATRICLIP GILLINOV-COSGROVE LAA CLIP received FDA 510(k) clearance on 2013-05-14, under 510(k) number K131107.

Who is the listed applicant for ATRICLIP GILLINOV-COSGROVE LAA CLIP?

The FDA 510(k) record lists AtriCure, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ATRICLIP GILLINOV-COSGROVE LAA CLIP?

The FDA product code for ATRICLIP GILLINOV-COSGROVE LAA CLIP is FZP.

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Other records listing AtriCure, Inc. as applicant

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Related Devices (Code: FZP)

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.

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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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