FDA 510(k)

Reprocessed Ethicon Bladeless Trocars; Reprocessed Ethicon Universal Trocar Sleeves

K-번호: K172097 · 2017-10-06

결정일2017-10-06

제품 코드NLM

자문 위원회GU

결정Substantially Equivalent

기기 요약

Reprocessed Ethicon Bladeless Trocars; Reprocessed Ethicon Universal Trocar Sleeves is the device name listed in this FDA 510(k) record. The listed applicant is Renovo, Inc.. It received FDA 510(k) clearance on 2017-10-06 under 510(k) number K172097. The device is classified under product code NLM. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

자주 묻는 질문

What is the Reprocessed Ethicon Bladeless Trocars; Reprocessed Ethicon Universal Trocar Sleeves?

Reprocessed Ethicon Bladeless Trocars; Reprocessed Ethicon Universal Trocar Sleeves is a medical device that received FDA 510(k) clearance on 2017-10-06. The listed applicant is Renovo, Inc.. The 510(k) number is K172097.

When did Reprocessed Ethicon Bladeless Trocars; Reprocessed Ethicon Universal Trocar Sleeves receive FDA 510(k) clearance?

Reprocessed Ethicon Bladeless Trocars; Reprocessed Ethicon Universal Trocar Sleeves received FDA 510(k) clearance on 2017-10-06, under 510(k) number K172097.

Who is the listed applicant for Reprocessed Ethicon Bladeless Trocars; Reprocessed Ethicon Universal Trocar Sleeves?

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

What is the FDA product code for Reprocessed Ethicon Bladeless Trocars; Reprocessed Ethicon Universal Trocar Sleeves?

The FDA product code for Reprocessed Ethicon Bladeless Trocars; Reprocessed Ethicon Universal Trocar Sleeves is NLM.

Renovo, Inc.를 신청인으로 등재한 기타 기록

K173740Reprocessed DePuy Mitek Ablation Wand K173741Reprocessed ArthoCare Ablation Wand K172647Reprocessed ArthroCare ENT Coblator K172093Reprocessed Covidien Trocar K172092Reprocessed Shavers/Burs

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