K950914 is an FDA 510(k) clearance for the RI-FORMER WALL MODEL 2,5 V/220 V OR 110 V 3,5 V/220 V OR 110 V, RI-FORMER ANAESTHETIC MODEL 2,5 V/220 V OR 110 C 3,5 V/V. This device is classified as a Ophthalmoscope, Battery-powered (Class II - Special Controls, product code HLJ).
Submitted by Rudolf Riester GmbH & Co. KG (D-72417 Jungingen, DE). The FDA issued a Cleared decision on July 24, 1995, 151 days after receiving the submission on February 23, 1995.
This device falls under the Ophthalmic FDA review panel. Regulated under 21 CFR 886.1570.
| 510(k) Number | K950914 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | February 23, 1995 |
| Decision Date | July 24, 1995 |
| Days to Decision | 151 days |
| Submission Type | Traditional |
| Review Panel | Ophthalmic (OP) |
| Summary | Statement |
| Product Code | HLJ — Ophthalmoscope, Battery-powered |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 886.1570 |