FDA 510(k)

APTOS 테이스 – 폴리프로필렌 수술 소겔

K-번호: K192953 · 2020-08-27

결정일2020-08-27

제품 코드GAW

자문 위원회SU

결정Substantially Equivalent

기기 요약

APTOS Threads – Polypropylene Surgical Sutures is the device name listed in this FDA 510(k) record. The listed applicant is Aptos, LLC. It received FDA 510(k) clearance on 2020-08-27 under 510(k) number K192953. The device is classified under product code GAW. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

자주 묻는 질문

What is the APTOS Threads – Polypropylene Surgical Sutures?

APTOS Threads – Polypropylene Surgical Sutures is a medical device that received FDA 510(k) clearance on 2020-08-27. The listed applicant is Aptos, LLC. The 510(k) number is K192953.

When did APTOS Threads – Polypropylene Surgical Sutures receive FDA 510(k) clearance?

APTOS Threads – Polypropylene Surgical Sutures received FDA 510(k) clearance on 2020-08-27, under 510(k) number K192953.

Who is the listed applicant for APTOS Threads – Polypropylene Surgical Sutures?

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

What is the FDA product code for APTOS Threads – Polypropylene Surgical Sutures?

The FDA product code for APTOS Threads – Polypropylene Surgical Sutures is GAW.

공식 출처

FDA 데이터베이스에서 보기 →

FDA Open API에서 수집된 데이터입니다. 가장 정확하고 공인된 정보는 항상 공식 레코드를 참조하시기 바랍니다.

APTOS 테이스 – 폴리프로필렌 수술 소겔

기기 요약

자주 묻는 질문

관련 임상시험

관련 기기 (코드: GAW)

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