Miami Eye Technology, Inc.
Mchenry, IL, US
Miami Eye Technology, Inc. appears in FDA device records in Mchenry, IL. FDA records list 6 510(k) clearances between and , no PMA records and no registered establishments. As of , FDA records show no recalls for this company.
FDA records held for this company
- 510(k) clearances
- 6
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 6 510(k) clearances for Miami Eye Technology, Inc. between 1983 and 1984. The busiest year on record is 1983, with 4. The most recent is 1984, with 2.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1983 | 4 |
| 1984 | 2 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K841101 | CLAYMAN-PAREL CAPSULE COUPEUR | HNY | Substantially Equivalent | |
| K832912 | GELENDER VACUUM FIXATION RING SYS | HNH | Substantially Equivalent | |
| K832996 | SURGICAL IOP MONITOR | HKY | Substantially Equivalent | |
| K832997 | EPA AUTOMATED INFUSION POLE | HQC | Substantially Equivalent | |
| K832911 | ABBOTT GLOBE HOLDER | HJO | Substantially Equivalent | |
| K831702 | RARE-EARTH INTRA-OCULAR MAGNET | HPN | Substantially Equivalent |
Registered establishments
No FDA establishment registrations recorded against this company.
FDA product codes
Recall records
No recall records for this company in the ingested FDA data.
Verification record
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Data as of , FDA export datePage updated Source: openFDA, public domain