FDA 510(k)

Solax Electric Scooter (Model: S202261B)

K-번호: K202549 · 2021-02-26

신청자Dongguan Prestige Sporting Goods Co., Ltd.

결정일2021-02-26

제품 코드INI

자문 위원회PM

결정Substantially Equivalent

기기 요약

Solax Electric Scooter (Model: S202261B) is the device name listed in this FDA 510(k) record. The listed applicant is Dongguan Prestige Sporting Goods Co., Ltd.. It received FDA 510(k) clearance on 2021-02-26 under 510(k) number K202549. 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 Solax Electric Scooter (Model: S202261B)?

Solax Electric Scooter (Model: S202261B) is a medical device that received FDA 510(k) clearance on 2021-02-26. The listed applicant is Dongguan Prestige Sporting Goods Co., Ltd.. The 510(k) number is K202549.

When did Solax Electric Scooter (Model: S202261B) receive FDA 510(k) clearance?

Solax Electric Scooter (Model: S202261B) received FDA 510(k) clearance on 2021-02-26, under 510(k) number K202549.

Who is the listed applicant for Solax Electric Scooter (Model: S202261B)?

The FDA 510(k) record lists Dongguan Prestige Sporting Goods Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Solax Electric Scooter (Model: S202261B)?

The FDA product code for Solax Electric Scooter (Model: S202261B) is INI.

Dongguan Prestige Sporting Goods Co., Ltd.를 신청인으로 등재한 기타 기록

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