American Medical Devices, Inc.
American Medical Devices, Inc. holds FDA 510(k) medical device clearances, first cleared 1997, most recent 1998.
Top product codes for American Medical Devices, Inc.
Recent clearances by American Medical Devices, Inc.
- K974561 — MOISTAIR FLUID AIR TUBING SET
- K971853 — ENDOVIEW SPPHIRE LENS SET
- K970882 — ENDOLIGHT END IRRIGATING ENDO-ILLUMINATOR (20 GA. AND 19 GA.)
- K970873 — ENDOSOFT SOFT TIP NEEDLE (20 GA. AND 19 GA.)
- K970875 — ENDOLIGHT FIBEROPTIC ENDO-ILLUMINATOR (20 GA. & 19 GA.)
- K970878 — ENDOLIGHT FIBEROPTIC REGULAR MONOFILAMENT AND FINE MONOFILAMENT
Data sourced from openFDA. This site is unofficial and independent of the FDA.