American Medical Devices, Inc.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 6
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K974561 | MOISTAIR FLUID AIR TUBING SET | February 19, 1998 |
| K971853 | ENDOVIEW SPPHIRE LENS SET | August 6, 1997 |
| K970882 | ENDOLIGHT END IRRIGATING ENDO-ILLUMINATOR (20 GA. AND 19 GA.) | June 24, 1997 |
| K970873 | ENDOSOFT SOFT TIP NEEDLE (20 GA. AND 19 GA.) | May 20, 1997 |
| K970875 | ENDOLIGHT FIBEROPTIC ENDO-ILLUMINATOR (20 GA. & 19 GA.) | May 20, 1997 |
| K970878 | ENDOLIGHT FIBEROPTIC REGULAR MONOFILAMENT AND FINE MONOFILAMENT | May 6, 1997 |