General Project
FDA Regulatory Profile
General Project appears in FDA public data with 0 recalls, 6 510(k) clearances, 2 FDA inspections, and 1 compliance action on record. Its most recent 510(k) clearance was granted on August 16, 2016.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 6
- Inspections
- 2
- Compliance Actions
- 1
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K161502 | MC1 Plus | August 16, 2016 |
| K091615 | MED CONTOUR | May 6, 2010 |
| K062312 | AXIOM PULSED LIGHT SYSTEM | October 16, 2006 |
| K053041 | MED SCULPT | August 2, 2006 |
| K051508 | MED FLASH II INTENSE PULSED LIGHT SYSTEM. | October 5, 2005 |
| K004014 | MD 30 COMPACT | March 16, 2001 |