K951132 is an FDA 510(k) clearance for the ANGIOSCAN (AS STAND ALONE INSTRUMENT). This device is classified as a Ophthalmoscope, Ac-powered (Class II - Special Controls, product code HLI).
Submitted by Carl Zeiss Meditec, Inc. (San Diego, US). The FDA issued a Cleared decision on June 26, 1995, 105 days after receiving the submission on March 13, 1995.
This device falls under the Ophthalmic FDA review panel. Regulated under 21 CFR 886.1570.
| 510(k) Number | K951132 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | March 13, 1995 |
| Decision Date | June 26, 1995 |
| Days to Decision | 105 days |
| Submission Type | Traditional |
| Review Panel | Ophthalmic (OP) |
| Summary | Summary PDF |
| Product Code | HLI — Ophthalmoscope, Ac-powered |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 886.1570 |