FDA Product Code
FDA Product Code HKL — Clearance Directory
- Device Class
- Class II
- Assigned Panel
- Ophthalmic
- 21 CFR Citation
- 886.1780
510(k) Clearances — 6 records
| K-Number | Device Name | Applicant | Decision Date | Clearance Type | Summary |
|---|---|---|---|---|---|
| K001111 | PANORET, MODEL 1000A | Cmt Medical Technologies, Ltd. | 2000-07-07 | Traditional | PDF ↗ |
| K950789 | STREAK RETINOSCOPE RX-1 | Neitz Instruments Company, Ltd. | 1995-03-28 | Traditional | PDF ↗ |
| K950790 | STREAK RETINOSCOPE RX-2 | Neitz Instruments Company, Ltd. | 1995-03-22 | Traditional | PDF ↗ |
| K893171 | VISTA STREAK RETINOSCOPE (AC-POWERED) | Keeler Instruments, Inc. | 1989-09-21 | Traditional | PDF ↗ |
| K812764 | KOI BLUE FIELD ENTOPTOSCOPE | Koi, Inc. | 1981-12-02 | Traditional | PDF ↗ |
| K800238 | MOIRE FRINGE VISOMETER AFTER LOTMAR | Hagg-Streit Service, Inc. | 1980-03-10 | Traditional | PDF ↗ |
Product code HKL · Class II · Ophthalmic. Data: openFDA.