Intl. Ophthalmic Industries Corp. - FDA 510(k) Cleared Devices
6
Total
6
Cleared
0
Denied
Intl. Ophthalmic Industries Corp. has 6 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 6 cleared submissions from 1979 to 1996. Primary specialty: Ophthalmic.
Browse the FDA 510(k) cleared devices submitted by Intl. Ophthalmic Industries Corp. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Intl. Ophthalmic Industries Corp.
6 devices
Cleared
Jul 23, 1996
MEGATRON OPHTHALMIC SURGICAL SYSTEM
Ophthalmic
85d
Cleared
Oct 31, 1989
DIATHRON(R) DIATHERMY UNIT
Ophthalmic
104d
Cleared
Oct 17, 1989
MAGNETRON MUNICH MODEL ELECTRONIC CONTROL UNIT
Ophthalmic
90d
Cleared
Oct 17, 1989
PHACOEMULSIFICATION UNIT TO REMOVE CATARAC. LENS
Ophthalmic
90d
Cleared
Apr 06, 1983
ASPITRON
Ophthalmic
169d
Cleared
Nov 05, 1979
(MICRO-KERATRON, MICRO DUCT TREPHINE)
Ophthalmic
61d