Miami Eye Technology, Inc.
Miami Eye Technology, Inc. appears in FDA public data with 0 recalls, 6 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on May 16, 1984.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 6
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K841101 | CLAYMAN-PAREL CAPSULE COUPEUR | May 16, 1984 |
| K832912 | GELENDER VACUUM FIXATION RING SYS | January 10, 1984 |
| K832996 | SURGICAL IOP MONITOR | November 28, 1983 |
| K832997 | EPA AUTOMATED INFUSION POLE | October 4, 1983 |
| K832911 | ABBOTT GLOBE HOLDER | September 29, 1983 |
| K831702 | RARE-EARTH INTRA-OCULAR MAGNET | June 30, 1983 |