FDA 510(k)

A08 전동轮椅

K-번호: K163204 · 2017-05-05

신청자Kunshan Aoshida Electric Technology Co., Ltd.

결정일2017-05-05

제품 코드ITI

자문 위원회PM

결정Substantially Equivalent

기기 요약

A08 Power wheelchair is the device name listed in this FDA 510(k) record. The listed applicant is Kunshan Aoshida Electric Technology Co., Ltd.. It received FDA 510(k) clearance on 2017-05-05 under 510(k) number K163204. The device is classified under product code ITI. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

자주 묻는 질문

What is the A08 Power wheelchair?

A08 Power wheelchair is a medical device that received FDA 510(k) clearance on 2017-05-05. The listed applicant is Kunshan Aoshida Electric Technology Co., Ltd.. The 510(k) number is K163204.

When did A08 Power wheelchair receive FDA 510(k) clearance?

A08 Power wheelchair received FDA 510(k) clearance on 2017-05-05, under 510(k) number K163204.

Who is the listed applicant for A08 Power wheelchair?

The FDA 510(k) record lists Kunshan Aoshida Electric Technology Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for A08 Power wheelchair?

The FDA product code for A08 Power wheelchair is ITI.

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A08 전동轮椅

기기 요약

자주 묻는 질문

관련 임상시험

관련 기기 (코드: ITI)

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