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Chiron Vision Corp.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
34
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K970727MPORT FOLDABLE LENS PLACEMENT SYSTEMDecember 17, 1997
K972808HANSATOME MICROKERATOMEOctober 24, 1997
K960414SYNERGIST POWER PACKApril 24, 1996
K944993IOLAB.SITE CD PHACOEMULSIFICATION MODULEOctober 12, 1995
K944995IOLAB/SITE PERISTALTIC MODULEOctober 5, 1995
K951292PASSPORT FOLDABLE LENS PLACEMENT SYSTEMJune 2, 1995
K944994IOLAB/SITE DISPOSABLE DIAPHRAGM CASSETTEMarch 14, 1995
K941550AUTOMATIC CORNEAL SHAPER SURGICAL INSTRUMENTNovember 22, 1994
K935233IOLAB LACRIMAL DUCT CATHETERSeptember 15, 1994
K925606OPTICAL ZONE/HEXAGONAL/ASTIGMATISM/RADIAL MARKERSAugust 29, 1994
K926412MICRON-SCOPE IIJuly 19, 1994
K932600MODIFIED SITE POWER HANDPIECE IIJanuary 25, 1994
K924198MODIFIED SITE FIBER OPTIC MODULENovember 23, 1992
K922595MODIFIED SITE MACROBORE PHACO NEEDLEAugust 31, 1992
K922996MODIFIED SITE DIAPHRAGM CASSETTE FOR OPHTHALMICSJuly 27, 1992
K921607IOLAB REUSABLE PERISTATIC CASSETTE/OPHTHALMIC USEJune 30, 1992
K922077MODIFIED SITE POWER HANDPIECEJune 23, 1992
K885164LASAG MICRORUPTOR 2 ND:YAG OPHTH. LASER SYSTEMJanuary 10, 1989
K883199MODIFICATION TO THE SITE PERISTALTIC MODULE SYSTEMSeptember 15, 1988
K871245LASER CONTACT LENSES CGA 1, CGI 1, CGP 1, CGV 1May 7, 1987