Koi, Inc.
FDA 510(k) & PMA Approved Devices — 7 products
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Total Devices7
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K843247 | KOI PACHYMETER | ITX | 1986-04-30 | View |
| 510(k) | K830366 | DIAMOND KNIFE | HNN | 1983-03-09 | View |
| 510(k) | K812764 | KOI BLUE FIELD ENTOPTOSCOPE | HKL | 1981-12-02 | View |
| 510(k) | K812450 | KOI DIAMOND KNIFE | HNN | 1981-09-21 | View |
| 510(k) | K812097 | KOI LACREMAL HOOK & DILATOR | HNW | 1981-08-18 | View |
| 510(k) | K812010 | KOI LACRIMAL INTUBATION SYSTEM | HMX | 1981-07-28 | View |
| 510(k) | K812011 | BLADE GAUGE | HOE | 1981-07-28 | View |
No matching devices.
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