Air Compression Therapy Device (K1002/K1006/K1007/K1008/K1061)— 510(k) K251623

Substantially Equivalent

Shenzhen Yicai Health Technology Co., Ltd.

FDA 510(k) clearance K251623 for Air Compression Therapy Device (K1002/K1006/K1007/K1008/K1061), Substantially Equivalent on 2025-09-17. Applicant: Shenzhen Yicai Health Technology Co., Ltd..

Clearance details

Applicant: Shenzhen Yicai Health Technology Co., Ltd.
Product code: Code IRP
Advisory panel: Physical Medicine
Date received: 2025-05-28
Decision date: 2025-09-17
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Shenzhen, CN

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