The following data is part of a premarket notification filed by F. & F. Koenigkramer with the FDA for Reliance Ophthalmic Slit Lamp R-083.
| Device ID | K834060 |
| 510k Number | K834060 |
| Device Name: | RELIANCE OPHTHALMIC SLIT LAMP R-083 |
| Classification | Laser, Ophthalmic |
| Applicant | F. & F. KOENIGKRAMER 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | HQF |
| CFR Regulation Number | 886.4390 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1983-11-25 |
| Decision Date | 1984-02-04 |