Chiron Vision Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Chiron Vision Corp. - FDA 510(k) Cleared Devices
34
Total
34
Cleared
0
Denied
Chiron Vision Corp. has 34 FDA 510(k) cleared ophthalmic devices. Based in Irvine, US.
Historical record: 34 cleared submissions from 1980 to 1997.
Browse the complete list of FDA 510(k) cleared ophthalmic devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Chiron Vision Corp.
34 devices
Cleared
Dec 17, 1997
MPORT FOLDABLE LENS PLACEMENT SYSTEM
Ophthalmic
292d
Cleared
Oct 24, 1997
HANSATOME MICROKERATOME
Ophthalmic
88d
Cleared
Apr 24, 1996
SYNERGIST POWER PACK
Ophthalmic
86d
Cleared
Oct 12, 1995
IOLAB.SITE CD PHACOEMULSIFICATION MODULE
Ophthalmic
365d
Cleared
Oct 05, 1995
IOLAB/SITE PERISTALTIC MODULE
Ophthalmic
358d
Cleared
Jun 02, 1995
PASSPORT FOLDABLE LENS PLACEMENT SYSTEM
Ophthalmic
72d
Cleared
Mar 14, 1995
IOLAB/SITE DISPOSABLE DIAPHRAGM CASSETTE
Ophthalmic
153d
Cleared
Nov 22, 1994
AUTOMATIC CORNEAL SHAPER SURGICAL INSTRUMENT
Ophthalmic
237d
Cleared
Sep 15, 1994
IOLAB LACRIMAL DUCT CATHETER
Ophthalmic
318d
Cleared
Aug 29, 1994
OPTICAL ZONE/HEXAGONAL/ASTIGMATISM/RADIAL MARKERS
Ophthalmic
662d
Cleared
Jul 19, 1994
MICRON-SCOPE II
Ophthalmic
575d
Cleared
Jan 25, 1994
MODIFIED SITE POWER HANDPIECE II
Dental
242d