Chiron Intraoptics is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Chiron Intraoptics - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
Chiron Intraoptics has 4 FDA 510(k) cleared medical devices. Based in Irvine, US.
Historical record: 4 cleared submissions from 1992 to 1993. Primary specialty: Ophthalmic.
Browse the FDA 510(k) cleared devices submitted by Chiron Intraoptics Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Chiron Intraoptics
4 devices
Cleared
Jul 29, 1993
PHACOTRON GOLD MULTIFUNCTION ULTRASONIC HANDPIECE
Ophthalmic
262d
Cleared
Oct 06, 1992
OPTISOL-GS CORNEAL STORAGE MEDIA
Ophthalmic
48d
Cleared
Jun 09, 1992
DEXSOL CORNEAL STORAGE MEDIA CONTAINER, MODIFIED
Ophthalmic
76d
Cleared
Jun 09, 1992
OPTISOL CORNEAL STORAGE MEDIA CONTAINER/MODIFIED
Ophthalmic
76d