FDA Product Code
FDA Product Code HKM — Clearance Directory
- Device Class
- Class I
- Assigned Panel
- Ophthalmic
- 21 CFR Citation
- 886.1780
510(k) Clearances — 7 records
| K-Number | Device Name | Applicant | Decision Date | Clearance Type | Summary |
|---|---|---|---|---|---|
| K964338 | RI-TINISCOPE-SLIT/RI-TINISCOPE SPOT/RI-VISION-SLIT/RI-VISION-SPOT | Rudolf Riester GmbH & Co. KG | 1997-01-09 | Traditional | PDF ↗ |
| K950795 | STREAK RETINOSCOPE RX-RP | Neitz Instruments Company, Ltd. | 1995-03-28 | Traditional | PDF ↗ |
| K950794 | STREAK RETINOSCOPE RX-RC | Neitz Instruments Company, Ltd. | 1995-03-28 | Traditional | PDF ↗ |
| K950792 | STREAK RETINOSCOPE RX-3A | Neitz Instruments Company, Ltd. | 1995-03-28 | Traditional | PDF ↗ |
| K950793 | SPOT RETINOSCOPE RX-3SP | Neitz Instruments Company, Ltd. | 1995-03-28 | Traditional | PDF ↗ |
| K950791 | STREAK RETINOSCOPE RX-3 | Neitz Instruments Company, Ltd. | 1995-03-28 | Traditional | PDF ↗ |
| K840840 | GENERATED RETINAL REFLEX IMAGERY SYS | Electro Optical Instruments | 1984-07-12 | Traditional | PDF ↗ |
Product code HKM · Class I · Ophthalmic. Data: openFDA.