Majestic Drug Co., Inc.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 3
- Inspections
- 3
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K101771 | RELINE-IT MODEL RELINE-IT | September 20, 2010 |
| K964773 | DENTEMP ONE STEP | February 21, 1997 |
| K821581 | DEN TEMP | June 14, 1982 |