Allergan Medical Optics
Allergan Medical Optics appears in FDA public data with 0 recalls, 7 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on June 15, 1995.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 7
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K951462 | AMO PROFINESSE III ULTRASONIC HANDPIECE SYSTEM | June 15, 1995 |
| K941603 | AMO PHACOFLEX INSERTER DISPOSABLE CARTRIDGE, AND HANDPIECE | July 6, 1994 |
| K930320 | AMO PHACOFLEX INSERTER, FOLDABLE IOL INSERT INSTR | April 7, 1994 |
| K925254 | AMO(R) FLRX-TIP(TM) DISPOS I/A HANDPIECE, OPO-38 | January 7, 1993 |
| K924235 | AMO ELITE | December 23, 1992 |
| K911998 | MULTITOME MODEL 1000, VITRECTOMY DRIVING SYSTEM | July 26, 1991 |
| K893199 | PHACO-INJECTOR(TM) INTRAOCULAR LENS IMPLANT INSTR | June 16, 1989 |