Aztec Medical Products, Inc.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 5
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
| K801939 | RHYTIDOMETER | September 26, 1980 |
| K801937 | BLEPHAROMETER | September 16, 1980 |
| K801938 | RHINOMETER | September 9, 1980 |
| K792608 | TEGTMEIER MAMMOMETER | January 4, 1980 |
| K791221 | TEGTMEIER MAMMOMETER | July 3, 1979 |