Chiron Vision Corp.
Chiron Vision Corp. appears in FDA public data with 0 recalls, 34 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on December 17, 1997.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 34
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K970727 | MPORT FOLDABLE LENS PLACEMENT SYSTEM | December 17, 1997 |
| K972808 | HANSATOME MICROKERATOME | October 24, 1997 |
| K960414 | SYNERGIST POWER PACK | April 24, 1996 |
| K944993 | IOLAB.SITE CD PHACOEMULSIFICATION MODULE | October 12, 1995 |
| K944995 | IOLAB/SITE PERISTALTIC MODULE | October 5, 1995 |
| K951292 | PASSPORT FOLDABLE LENS PLACEMENT SYSTEM | June 2, 1995 |
| K944994 | IOLAB/SITE DISPOSABLE DIAPHRAGM CASSETTE | March 14, 1995 |
| K941550 | AUTOMATIC CORNEAL SHAPER SURGICAL INSTRUMENT | November 22, 1994 |
| K935233 | IOLAB LACRIMAL DUCT CATHETER | September 15, 1994 |
| K925606 | OPTICAL ZONE/HEXAGONAL/ASTIGMATISM/RADIAL MARKERS | August 29, 1994 |
| K926412 | MICRON-SCOPE II | July 19, 1994 |
| K932600 | MODIFIED SITE POWER HANDPIECE II | January 25, 1994 |
| K924198 | MODIFIED SITE FIBER OPTIC MODULE | November 23, 1992 |
| K922595 | MODIFIED SITE MACROBORE PHACO NEEDLE | August 31, 1992 |
| K922996 | MODIFIED SITE DIAPHRAGM CASSETTE FOR OPHTHALMICS | July 27, 1992 |
| K921607 | IOLAB REUSABLE PERISTATIC CASSETTE/OPHTHALMIC USE | June 30, 1992 |
| K922077 | MODIFIED SITE POWER HANDPIECE | June 23, 1992 |
| K885164 | LASAG MICRORUPTOR 2 ND:YAG OPHTH. LASER SYSTEM | January 10, 1989 |
| K883199 | MODIFICATION TO THE SITE PERISTALTIC MODULE SYSTEM | September 15, 1988 |
| K871245 | LASER CONTACT LENSES CGA 1, CGI 1, CGP 1, CGV 1 | May 7, 1987 |