American Optical Corp. - FDA 510(k) Cleared Devices
35
Total
35
Cleared
0
Denied
American Optical Corp. has 35 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 35 cleared submissions from 1976 to 1995. Primary specialty: Ophthalmic.
Browse the FDA 510(k) cleared devices submitted by American Optical Corp. Filter by specialty or product code using the sidebar.
35 devices
Cleared
Sep 06, 1995
PHACO TIP
Ophthalmic
191d
Cleared
May 26, 1995
AOI UNIVERSAL ULTRASONIC HANDPIECE
Ophthalmic
88d
Cleared
Feb 22, 1994
P4000 PHACOEMULSIFIER
Ophthalmic
342d
Cleared
Feb 22, 1994
AORP4000 REUSABLE PAK
Ophthalmic
342d
Cleared
Jan 25, 1994
AOD4000 DISPOSABLE PAK
Ophthalmic
314d
Cleared
Apr 01, 1982
FLEXIBLE PROCTOSIGMOIDOSCOPE, #FPS-3
Gastroenterology & Urology
9d
Cleared
Dec 29, 1981
TISSUE PROCESSING CASSETTES & ACCESS
Pathology
21d
Cleared
Nov 02, 1981
MODEL SC-6, FLEXIBLE SIAMOIDOSCOPE
Gastroenterology & Urology
11d
Cleared
Sep 08, 1981
PHOTOLITE AOLITE TINTOMATIC LENS
Ophthalmic
49d
Cleared
Aug 18, 1981
SR-1V DATA PRINTER
Ophthalmic
28d
Cleared
Jun 23, 1981
MODEL FUS-1, FLEXIBLE URETEROSCOPE
Gastroenterology & Urology
22d
Cleared
May 15, 1981
ULTRAMATIC PROJECT-O-CHART OPHTH. PROJ
Ophthalmic
17d