Accelerated Care Plus
FDA 510(k) & PMA Approved Devices — 2 products
Advertisement
Total Devices2
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K153456 | Megapulse III Shortwave Diathermy | IMJ | 2016-06-14 | View |
| 510(k) | K093600 | OMNISTIM CONTINENCE+ PELVIC FLOOR STIMULATION SYSTEM | KPI | 2009-12-04 | View |
No matching devices.
Advertisement