FDA 510(k)

Mobility Scooter (Models: W3431Q, W3431R)

K-번호: K222507 · 2023-02-28

신청자Zhejiang Innuovo Rehabilitation Devices Co.,Ltd

결정일2023-02-28

제품 코드INI

자문 위원회PM

결정Substantially Equivalent

기기 요약

Mobility Scooter (Models: W3431Q, W3431R) is the device name listed in this FDA 510(k) record. The listed applicant is Zhejiang Innuovo Rehabilitation Devices Co.,Ltd. It received FDA 510(k) clearance on 2023-02-28 under 510(k) number K222507. The device is classified under product code INI. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

자주 묻는 질문

What is the Mobility Scooter (Models: W3431Q, W3431R)?

Mobility Scooter (Models: W3431Q, W3431R) is a medical device that received FDA 510(k) clearance on 2023-02-28. The listed applicant is Zhejiang Innuovo Rehabilitation Devices Co.,Ltd. The 510(k) number is K222507.

When did Mobility Scooter (Models: W3431Q, W3431R) receive FDA 510(k) clearance?

Mobility Scooter (Models: W3431Q, W3431R) received FDA 510(k) clearance on 2023-02-28, under 510(k) number K222507.

Who is the listed applicant for Mobility Scooter (Models: W3431Q, W3431R)?

The FDA 510(k) record lists Zhejiang Innuovo Rehabilitation Devices Co.,Ltd as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Mobility Scooter (Models: W3431Q, W3431R)?

The FDA product code for Mobility Scooter (Models: W3431Q, W3431R) is INI.

Zhejiang Innuovo Rehabilitation Devices Co.,Ltd를 신청인으로 등재한 기타 기록

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