FDA 510(k)

Wrinkle Treatment Device (JM2)

K-번호: K240360 · 2024-04-05

결정일2024-04-05

제품 코드OHS

자문 위원회SU

결정Substantially Equivalent

기기 요약

Wrinkle Treatment Device (JM2) is the device name listed in this FDA 510(k) record. The listed applicant is Shenzhen Qianyu Technology Co., Ltd.. It received FDA 510(k) clearance on 2024-04-05 under 510(k) number K240360. The device is classified under product code OHS. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

자주 묻는 질문

What is the Wrinkle Treatment Device (JM2)?

Wrinkle Treatment Device (JM2) is a medical device that received FDA 510(k) clearance on 2024-04-05. The listed applicant is Shenzhen Qianyu Technology Co., Ltd.. The 510(k) number is K240360.

When did Wrinkle Treatment Device (JM2) receive FDA 510(k) clearance?

Wrinkle Treatment Device (JM2) received FDA 510(k) clearance on 2024-04-05, under 510(k) number K240360.

Who is the listed applicant for Wrinkle Treatment Device (JM2)?

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

What is the FDA product code for Wrinkle Treatment Device (JM2)?

The FDA product code for Wrinkle Treatment Device (JM2) is OHS.

Shenzhen Qianyu Technology Co., Ltd.를 신청인으로 등재한 기타 기록

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