Accelerated Care Plus Corp.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 3
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K153456 | Megapulse III Shortwave Diathermy | June 14, 2016 |
| K093600 | OMNISTIM CONTINENCE+ PELVIC FLOOR STIMULATION SYSTEM | December 4, 2009 |
| K060191 | ACP OMNIPAD LIGHT THERAPY SYSTEM & ACP OMNIPAD 500 CONTROL UNIT | July 12, 2006 |