Company ยท US
American Medical Devices, Inc.
FDA 510(k) clearances and medical device recalls filed under this name, 1997 to 1998. Name variants (Inc, Corp, punctuation) are merged.
6510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)
Product codes
Latest 510(k) clearances
| Decided | 510(k) | Device and applicant | Code |
|---|---|---|---|
| Feb 19, 1998 | K974561 | MOISTAIR FLUID AIR TUBING SET American Medical Devices, Inc. | KYG |
| Aug 6, 1997 | K971853 | ENDOVIEW SPPHIRE LENS SET American Medical Devices, Inc. | HJK |
| Jun 24, 1997 | K970882 | ENDOLIGHT END IRRIGATING ENDO-ILLUMINATOR (20 GA. AND 19 GA.) American Medical Devices, Inc. | MPA |
| May 20, 1997 | K970875 | ENDOLIGHT FIBEROPTIC ENDO-ILLUMINATOR (20 GA. & 19 GA.) American Medical Devices, Inc. | MPA |
| May 20, 1997 | K970873 | ENDOSOFT SOFT TIP NEEDLE (20 GA. AND 19 GA.) American Medical Devices, Inc. | HMX |
| May 6, 1997 | K970878 | ENDOLIGHT FIBEROPTIC REGULAR MONOFILAMENT AND FINE MONOFILAMENT American Medical Devices, Inc. | MPA |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||