Chiron Intraoptics
Chiron Intraoptics appears in FDA public data with 0 recalls, 4 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on July 29, 1993.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 4
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K925631 | PHACOTRON GOLD MULTIFUNCTION ULTRASONIC HANDPIECE | July 29, 1993 |
| K924165 | OPTISOL-GS CORNEAL STORAGE MEDIA | October 6, 1992 |
| K921729 | OPTISOL CORNEAL STORAGE MEDIA CONTAINER/MODIFIED | June 9, 1992 |
| K921728 | DEXSOL CORNEAL STORAGE MEDIA CONTAINER, MODIFIED | June 9, 1992 |