FDA 510(k)

Tuttnauer 수평 모델: 4472, 5596, 6690, 66120, 69120 및 69180 자동소독기

K-번호: K181456 · 2019-07-08

결정일2019-07-08

제품 코드FLE

자문 위원회HO

결정Substantially Equivalent

기기 요약

Tuttnauer Horizontal Models:4472,5596,6690,66120,69120 and 69180 autoclaves is the device name listed in this FDA 510(k) record. The listed applicant is Tuttnauer , Ltd.. It received FDA 510(k) clearance on 2019-07-08 under 510(k) number K181456. The device is classified under product code FLE. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

자주 묻는 질문

What is the Tuttnauer Horizontal Models:4472,5596,6690,66120,69120 and 69180 autoclaves?

Tuttnauer Horizontal Models:4472,5596,6690,66120,69120 and 69180 autoclaves is a medical device that received FDA 510(k) clearance on 2019-07-08. The listed applicant is Tuttnauer , Ltd.. The 510(k) number is K181456.

When did Tuttnauer Horizontal Models:4472,5596,6690,66120,69120 and 69180 autoclaves receive FDA 510(k) clearance?

Tuttnauer Horizontal Models:4472,5596,6690,66120,69120 and 69180 autoclaves received FDA 510(k) clearance on 2019-07-08, under 510(k) number K181456.

Who is the listed applicant for Tuttnauer Horizontal Models:4472,5596,6690,66120,69120 and 69180 autoclaves?

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

What is the FDA product code for Tuttnauer Horizontal Models:4472,5596,6690,66120,69120 and 69180 autoclaves?

The FDA product code for Tuttnauer Horizontal Models:4472,5596,6690,66120,69120 and 69180 autoclaves is FLE.

Tuttnauer , Ltd.를 신청인으로 등재한 기타 기록

K222608Tuttnauer Pre-vacuum Steam Sterilizer models 3870HSG and 3870HSG-WS K221227Tuttnauer Horizontal autoclave series model: 4472, 5596, 6690, 66120 K213080T-Edge 10, T-Edge 11

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