Keeler Optical Products , Ltd. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Keeler Optical Products , Ltd. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Keeler Optical Products , Ltd. has 5 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 5 cleared submissions from 1978 to 1981. Primary specialty: Ophthalmic.
Browse the FDA 510(k) cleared devices submitted by Keeler Optical Products , Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Keeler Optical Products , Ltd.
5 devices
Cleared
May 13, 1981
KEELER/KONAN SPECULAR MICROSCOPE
Ophthalmic
84d
Cleared
Jul 21, 1980
KEELER AMOILS ACULL CRYO OPHTHALMIC UNIT
Ophthalmic
34d
Cleared
Dec 11, 1979
NEVYAS AUTOPRESS EYE COMPRESSOR
Ophthalmic
32d
Cleared
Jan 26, 1979
LEVIGATOR, KEELER PHOKO
Ophthalmic
30d
Cleared
Dec 04, 1978
LOCATOR, FOREIGN BODY
Ophthalmic
26d