Air compression massager (ACM-PLUS-A1, ACM-PLUS-A2, ACM-PLUS-A3, ACM-PLUS-A4, ACM-PLUS-A5, ACM-PLUS-A6)— 510(k) K243206
Substantially EquivalentSichuan Qianli-Beoka Medical Technology, Inc.
FDA 510(k) clearance K243206 for Air compression massager (ACM-PLUS-A1, ACM-PLUS-A2, ACM-PLUS-A3, ACM-PLUS-A4, ACM-PLUS-A5, ACM-PLUS-A6), Substantially Equivalent on 2025-02-19. Applicant: Sichuan Qianli-Beoka Medical Technology, Inc.. Device class: 2.
Clearance details
- Applicant
- Sichuan Qianli-Beoka Medical Technology, Inc.
- Product code
- Code IRP
- Device class
- Class 2
- Regulation
- 21 CFR 890.5650
- Advisory panel
- Physical Medicine
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Chengdu, CN
Recent devices under product code IRP
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