FDA 510(k)

Weely Manual Wheelchair

K-번호: K152827 · 2016-02-19

결정일2016-02-19

제품 코드IOR

자문 위원회PM

결정Substantially Equivalent

기기 요약

Weely Manual Wheelchair is the device name listed in this FDA 510(k) record. The listed applicant is Rupiani. It received FDA 510(k) clearance on 2016-02-19 under 510(k) number K152827. The device is classified under product code IOR. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

자주 묻는 질문

What is the Weely Manual Wheelchair?

Weely Manual Wheelchair is a medical device that received FDA 510(k) clearance on 2016-02-19. The listed applicant is Rupiani. The 510(k) number is K152827.

When did Weely Manual Wheelchair receive FDA 510(k) clearance?

Weely Manual Wheelchair received FDA 510(k) clearance on 2016-02-19, under 510(k) number K152827.

Who is the listed applicant for Weely Manual Wheelchair?

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

What is the FDA product code for Weely Manual Wheelchair?

The FDA product code for Weely Manual Wheelchair is IOR.

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Weely Manual Wheelchair

기기 요약

자주 묻는 질문

관련 임상시험

관련 기기 (코드: IOR)

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