Stereo Optical Co., Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Stereo Optical Co., Inc. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Stereo Optical Co., Inc. has 5 FDA 510(k) cleared medical devices. Based in Chicago, US.
Historical record: 5 cleared submissions from 1984 to 1993. Primary specialty: Ophthalmic.
Browse the FDA 510(k) cleared devices submitted by Stereo Optical Co., Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Stereo Optical Co., Inc.
5 devices
Cleared
Apr 06, 1993
OPTEC 3000
Ophthalmic
196d
Cleared
Jan 18, 1991
OPTEC 2300 AFVT, ARMED FORCES VISION TESTER
Ophthalmic
86d
Cleared
Mar 17, 1988
OPTEC 1000 DMV VISION TESTER MODIFY
Ophthalmic
86d
Cleared
Nov 10, 1986
OPTEC 1000 DMV
Ophthalmic
62d
Cleared
Oct 05, 1984
VISION TESTER
Ophthalmic
64d