Company ยท US
Koi, Inc.
FDA 510(k) clearances and medical device recalls filed under this name, 1981 to 1986. Name variants (Inc, Corp, punctuation) are merged.
7510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)
Product codes
Latest 510(k) clearances
| Decided | 510(k) | Device and applicant | Code |
|---|---|---|---|
| Apr 30, 1986 | K843247 | KOI PACHYMETER Koi, Inc. | ITX |
| Mar 9, 1983 | K830366 | DIAMOND KNIFE Koi, Inc. | HNN |
| Dec 2, 1981 | K812764 | KOI BLUE FIELD ENTOPTOSCOPE Koi, Inc. | HKL |
| Sep 21, 1981 | K812450 | KOI DIAMOND KNIFE Koi, Inc. | HNN |
| Aug 18, 1981 | K812097 | KOI LACREMAL HOOK & DILATOR Koi, Inc. | HNW |
| Jul 28, 1981 | K812011 | BLADE GAUGE Koi, Inc. | HOE |
| Jul 28, 1981 | K812010 | KOI LACRIMAL INTUBATION SYSTEM Koi, Inc. | HMX |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||