FDA 510(k)

3MTM 앳естTM 레이드 5 스팀-플러스 테스트 팩

K-번호: K200536 · 2020-06-01

결정일2020-06-01

제품 코드FRC

자문 위원회HO

결정Substantially Equivalent

기기 요약

3MTM AttestTM Rapid 5 Steam-Plus Test Pack is the device name listed in this FDA 510(k) record. The listed applicant is 3M Complany. It received FDA 510(k) clearance on 2020-06-01 under 510(k) number K200536. The device is classified under product code FRC. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

자주 묻는 질문

What is the 3MTM AttestTM Rapid 5 Steam-Plus Test Pack?

3MTM AttestTM Rapid 5 Steam-Plus Test Pack is a medical device that received FDA 510(k) clearance on 2020-06-01. The listed applicant is 3M Complany. The 510(k) number is K200536.

When did 3MTM AttestTM Rapid 5 Steam-Plus Test Pack receive FDA 510(k) clearance?

3MTM AttestTM Rapid 5 Steam-Plus Test Pack received FDA 510(k) clearance on 2020-06-01, under 510(k) number K200536.

Who is the listed applicant for 3MTM AttestTM Rapid 5 Steam-Plus Test Pack?

The FDA 510(k) record lists 3M Complany as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for 3MTM AttestTM Rapid 5 Steam-Plus Test Pack?

The FDA product code for 3MTM AttestTM Rapid 5 Steam-Plus Test Pack is FRC.

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3MTM 앳естTM 레이드 5 스팀-플러스 테스트 팩

기기 요약

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관련 임상시험

관련 기기 (코드: FRC)

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