Medical Device Manufacturer · US , Atlanta , GA

American Medical Devices, Inc. - FDA 510(k) Cleared Devices

6 submissions · 6 cleared · Since 1997
6
Total
6
Cleared
0
Denied

American Medical Devices, Inc. has 6 FDA 510(k) cleared medical devices. Based in Atlanta, US.

Historical record: 6 cleared submissions from 1997 to 1998. Primary specialty: Ophthalmic.

Browse the FDA 510(k) cleared devices submitted by American Medical Devices, Inc. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - American Medical Devices, Inc.
6 devices
1-6 of 6
Cleared Feb 19, 1998
MOISTAIR FLUID AIR TUBING SET
K974561 · KYG
Ophthalmic · 76d
Cleared Aug 06, 1997
ENDOVIEW SPPHIRE LENS SET
K971853 · HJK
Ophthalmic · 78d
Cleared Jun 24, 1997
ENDOLIGHT END IRRIGATING ENDO-ILLUMINATOR (20 GA. AND 19 GA.)
K970882 · MPA
Ophthalmic · 106d
Cleared May 20, 1997
ENDOSOFT SOFT TIP NEEDLE (20 GA. AND 19 GA.)
K970873 · HMX
Ophthalmic · 71d
Cleared May 20, 1997
ENDOLIGHT FIBEROPTIC ENDO-ILLUMINATOR (20 GA. & 19 GA.)
K970875 · MPA
Ophthalmic · 71d
Cleared May 06, 1997
ENDOLIGHT FIBEROPTIC REGULAR MONOFILAMENT AND FINE MONOFILAMENT
K970878 · MPA
Ophthalmic · 57d
Filters
Filter by Specialty
All6 Ophthalmic 6