FDA 510(k)

AtriClip LAA Exclusion System with preloaded Gillinov-Cosgrove PRO V Clip

K番号: K153500 · 2016-01-27

決定日2016-01-27

製品コードFZP

諮問委員会SU （以下のテキストは翻訳されていません。） Policy: medical-regulatory-v1

決定大幅同等

医療機器の概要

AtriClip LAA Exclusion System with preloaded Gillinov-Cosgrove PRO V 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 2016-01-27 under 510(k) number K153500. The device is classified under product code FZP. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

よくある質問

What is the AtriClip LAA Exclusion System with preloaded Gillinov-Cosgrove PRO V Clip?

AtriClip LAA Exclusion System with preloaded Gillinov-Cosgrove PRO V Clip is a medical device that received FDA 510(k) clearance on 2016-01-27. The listed applicant is AtriCure, Inc.. The 510(k) number is K153500.

When did AtriClip LAA Exclusion System with preloaded Gillinov-Cosgrove PRO V Clip receive FDA 510(k) clearance?

AtriClip LAA Exclusion System with preloaded Gillinov-Cosgrove PRO V Clip received FDA 510(k) clearance on 2016-01-27, under 510(k) number K153500.

Who is the listed applicant for AtriClip LAA Exclusion System with preloaded Gillinov-Cosgrove PRO V 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 LAA Exclusion System with preloaded Gillinov-Cosgrove PRO V Clip?

The FDA product code for AtriClip LAA Exclusion System with preloaded Gillinov-Cosgrove PRO V Clip is FZP.

申請者としてAtriCure, Inc.を記載するその他の記録

K252056Isolator® Synergy™ EnCompass Clamp and Guide system（OLH、OSH、GPM100）K250371cryoICE cryoXT 冷凝固切除探头（cryoXT）K243860AtriClip PRO-Mini LAA Exclusion System (PROM)K243157AtriCure cryoICE BOX (ACM)K234151隔離シンエラシー・エンキャプチャー消融システム（EMH）K234125AtriClip FLEX-Mini LAA Exclusion System (ACHM)

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