HKL — Retinoscope, Ac-Powered Class II
FDA Device Classification
Classification Details
- Product Code
- HKL
- Device Class
- Class II
- Regulation Number
- 886.1780
- Submission Type
- Review Panel
- OP
- Medical Specialty
- Ophthalmic
- Implant
- No
Recent 510(k) Clearances
| K-Number | Applicant | Device Name | Date |
|---|
| K001111 | cmt medical technologies | PANORET, MODEL 1000A | July 7, 2000 |
| K950789 | neitz instruments company | STREAK RETINOSCOPE RX-1 | March 28, 1995 |
| K950790 | neitz instruments company | STREAK RETINOSCOPE RX-2 | March 22, 1995 |
| K893171 | keeler instruments | VISTA STREAK RETINOSCOPE (AC-POWERED) | September 21, 1989 |
| K812764 | koi | KOI BLUE FIELD ENTOPTOSCOPE | December 2, 1981 |
| K800238 | hagg-streit service | MOIRE FRINGE VISOMETER AFTER LOTMAR | March 10, 1980 |