The following data is part of a premarket notification filed by Koi, Inc. with the FDA for Koi Blue Field Entoptoscope.
| Device ID | K812764 |
| 510k Number | K812764 |
| Device Name: | KOI BLUE FIELD ENTOPTOSCOPE |
| Classification | Retinoscope, Ac-powered |
| Applicant | KOI, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | HKL |
| CFR Regulation Number | 886.1780 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1981-10-02 |
| Decision Date | 1981-12-02 |