Coburn Optical Ind., Inc. - FDA 510(k) Cleared Devices
14
Total
14
Cleared
0
Denied
Coburn Optical Ind., Inc. has 14 FDA 510(k) cleared ophthalmic devices. Based in Mchenry, US.
Historical record: 14 cleared submissions from 1978 to 1989.
Browse the complete list of FDA 510(k) cleared ophthalmic devices from this manufacturer. Filter by specialty or product code using the sidebar.
14 devices
Cleared
May 26, 1989
MAGNILINK SYSTEM 101
Ophthalmic
51d
Cleared
May 26, 1989
MAGNILINK SYSTEM 201
Ophthalmic
51d
Cleared
May 26, 1989
MAGNILINK SYSTEM 209
Ophthalmic
51d
Cleared
May 26, 1989
MAGNILINK SYSTEM 402/5
Ophthalmic
51d
Cleared
May 26, 1989
MAGNILINK SYSTEM 602
Ophthalmic
51d
Cleared
Aug 21, 1986
IRRIGATION & ASPIRATION/VITRECTOMY DEVICE
Ophthalmic
73d
Cleared
Oct 15, 1985
COBURN I/A SYSTEM
Ophthalmic
60d
Cleared
Jul 02, 1982
DISP. MICROSURGICAL KNIVES
General & Plastic Surgery
18d
Cleared
Oct 06, 1981
DI-CROWN
Ophthalmic
41d
Cleared
Feb 04, 1981
AUTOMATED PERIMETERS
Ophthalmic
58d
Cleared
Sep 09, 1980
BIOPHTAL CLINICAL ENDOTHELIAL MICROSCOPE
Ophthalmic
50d
Cleared
Jul 21, 1980
EYE-VAC
Ophthalmic
55d
Cleared
Oct 11, 1979
MEDITEC (RODENSTOCK) LASER PHOTOCOAGUL
Radiology
50d
Cleared
Nov 15, 1978
RETINOMETER
Ophthalmic
75d