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Air compression massager (ACM-PLUS-A1 +5 more)
FDA 510(k)Class II (US FDA 510(k))
510(k) K243206
Identifiers
- 510(k) Number
- K243206 FDA 510(k)
- FDA Product Code
- IRP FDA 510(k)
- Models / Variants
- ACM-PLUS-A1 FDA 510(k)ACM-PLUS-A2 FDA 510(k)ACM-PLUS-A3 FDA 510(k)ACM-PLUS-A4 FDA 510(k)ACM-PLUS-A5 FDA 510(k)ACM-PLUS-A6 FDA 510(k)
Classification
- Device Class
- Class II FDA 510(k)
- Legislation / Framework
- 21 CFR Part 890.5650 FDA 510(k)
- Regulation Number
- 890.5650 FDA 510(k)
- Advisory Committee
- Physical Medicine FDA 510(k)
- FDA Decision
- SESE Substantially Equivalent FDA 510(k)
Air compression massager (ACM-PLUS-A1 +5 more) by Sichuan Qianli-Beoka Medical Technology, Inc. — Class II — FDA_510K — listed in FDA 510(k) — 6 models
Authorization Coverage (1 country)
Regulatory Authorizations
United States Active
FDA_510K
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA 510(k) | United States | FDA_510K | K243206 | Class II | Active |
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Manufacturer
- Manufacturer
- Sichuan Qianli-Beoka Medical Technology, Inc.
Sources (1)
- FDA 510(k) K243206 24 fields · synced Jun 18, 2026