Cleaner Plus™ 혈전 제거 시스템, Cleaner Plus™ 흡수 캐터터, Cleaner Plus™ 65cm Maceration Wire를 포함한 Cleaner Plus™ 핸드피스, Cleaner Plus™ 135cm Maceration Wire를 포함한 Cleaner Plus™ 핸드피스, Cleaner Plus™ 흡수 컨테이너

Cleaner Plus™ Thrombectomy System, Cleaner Plus™ Aspiration Catheter, Cleaner Plus™ Handpiece with 65cm Maceration Wire, Cleaner Plus™ Handpiece with 135cm Maceration Wire, Cleaner Plus™ Aspiration Canister is a medical device that received FDA 510(k) clearance on 2023-04-10. The listed applicant is Argon Medical Devices, Inc.. The 510(k) number is K223176.

Cleaner Plus™ Thrombectomy System, Cleaner Plus™ Aspiration Catheter, Cleaner Plus™ Handpiece with 65cm Maceration Wire, Cleaner Plus™ Handpiece with 135cm Maceration Wire, Cleaner Plus™ Aspiration Canister received FDA 510(k) clearance on 2023-04-10, under 510(k) number K223176.

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

The FDA product code for Cleaner Plus™ Thrombectomy System, Cleaner Plus™ Aspiration Catheter, Cleaner Plus™ Handpiece with 65cm Maceration Wire, Cleaner Plus™ Handpiece with 135cm Maceration Wire, Cleaner Plus™ Aspiration Canister is KRA.