← Back to catalogue
Electronic Sphygmomanometers, Model: X1, X2, X5, X6, X7, X8, X11)
FDA 510(k)Class II (US FDA 510(k))
510(k) K221040
Identifiers
- 510(k) Number
- K221040 FDA 510(k)
- FDA Product Code
- DXN FDA 510(k)
Classification
- Device Class
- Class II FDA 510(k)
- Legislation / Framework
- 21 CFR Part 870.1130 FDA 510(k)
- Regulation Number
- 870.1130 FDA 510(k)
- Advisory Committee
- Cardiovascular FDA 510(k)
- FDA Decision
- SESE Substantially Equivalent FDA 510(k)
Electronic Sphygmomanometers, Model: X1, X2, X5, X6, X7, X8, X11) by Jiangxi Aicare Medical Technology Co., Ltd — Class II — FDA_510K — listed in FDA 510(k)
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 | K221040 | Class II | Active |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Jiangxi Aicare Medical Technology Co., Ltd
- FDA Applicant
- Jiangxi Aicare Medical Technology Co., Ltd.
Sources (1)
- FDA 510(k) K221040 24 fields · synced Jun 19, 2026