Koi, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
7
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K843247KOI PACHYMETERApril 30, 1986
K830366DIAMOND KNIFEMarch 9, 1983
K812764KOI BLUE FIELD ENTOPTOSCOPEDecember 2, 1981
K812450KOI DIAMOND KNIFESeptember 21, 1981
K812097KOI LACREMAL HOOK & DILATORAugust 18, 1981
K812011BLADE GAUGEJuly 28, 1981
K812010KOI LACRIMAL INTUBATION SYSTEMJuly 28, 1981