Amdia Medical Products
FDA Regulatory Profile
Amdia Medical Products appears in FDA public data with 0 recalls, 6 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on August 10, 1979.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 6
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K791333 | BOWLES STETHOSCOPE | August 10, 1979 |
| K791338 | DUAL HEAD STETHOSCOPE | August 10, 1979 |
| K791334 | MULTISCOPE | August 10, 1979 |
| K791335 | NURSESCOPE | August 10, 1979 |
| K791337 | TAYLOR NEUROLOGICAL HAMMER | August 3, 1979 |
| K791336 | BUCKS NEUROLOGICAL HAMMER | August 3, 1979 |