Chiron Vision Corp.
FDA 510(k) & PMA Approved Devices — 34 products
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Total Devices34
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K970727 | MPORT FOLDABLE LENS PLACEMENT SYSTEM | MSS | 1997-12-17 | View |
| 510(k) | K972808 | HANSATOME MICROKERATOME | HNO | 1997-10-24 | View |
| 510(k) | K960414 | SYNERGIST POWER PACK | HQC | 1996-04-24 | View |
| 510(k) | K944993 | IOLAB.SITE CD PHACOEMULSIFICATION MODULE | HQC | 1995-10-12 | View |
| 510(k) | K944995 | IOLAB/SITE PERISTALTIC MODULE | HQC | 1995-10-05 | View |
| 510(k) | K951292 | PASSPORT FOLDABLE LENS PLACEMENT SYSTEM | KYB | 1995-06-02 | View |
| 510(k) | K944994 | IOLAB/SITE DISPOSABLE DIAPHRAGM CASSETTE | HQC | 1995-03-14 | View |
| 510(k) | K941550 | AUTOMATIC CORNEAL SHAPER SURGICAL INSTRUMENT | HNO | 1994-11-22 | View |
| 510(k) | K935233 | IOLAB LACRIMAL DUCT CATHETER | OKS | 1994-09-15 | View |
| 510(k) | K925606 | OPTICAL ZONE/HEXAGONAL/ASTIGMATISM/RADIAL MARKERS | HMR | 1994-08-29 | View |
| 510(k) | K926412 | MICRON-SCOPE II | HMS | 1994-07-19 | View |
| 510(k) | K932600 | MODIFIED SITE POWER HANDPIECE II | EKX | 1994-01-25 | View |
| 510(k) | K924198 | MODIFIED SITE FIBER OPTIC MODULE | FCT | 1992-11-23 | View |
| 510(k) | K922595 | MODIFIED SITE MACROBORE PHACO NEEDLE | HQC | 1992-08-31 | View |
| 510(k) | K922996 | MODIFIED SITE DIAPHRAGM CASSETTE FOR OPHTHALMICS | KYG | 1992-07-27 | View |
| 510(k) | K921607 | IOLAB REUSABLE PERISTATIC CASSETTE/OPHTHALMIC USE | HQC | 1992-06-30 | View |
| 510(k) | K922077 | MODIFIED SITE POWER HANDPIECE | EKX | 1992-06-23 | View |
| 510(k) | K885164 | LASAG MICRORUPTOR 2 ND:YAG OPHTH. LASER SYSTEM | HQF | 1989-01-10 | View |
| 510(k) | K883199 | MODIFICATION TO THE SITE PERISTALTIC MODULE SYSTEM | HQC | 1988-09-15 | View |
| 510(k) | K871245 | LASER CONTACT LENSES CGA 1, CGI 1, CGP 1, CGV 1 | LQJ | 1987-05-07 | View |
No matching devices.
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