Medical Device Resource Corp.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 2
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K092284 | LIPISYSTEMS AQUAVAGE, MODELS AV2000 AND AV1200 | September 1, 2009 |
| K081593 | POWER ASPIRATOR, MODEL LS2 OR LS2DP | July 23, 2008 |