K945591 is an FDA 510(k) clearance for the APPLIED MEDICAL OPTICAL VALVULOTOME. This device is classified as a Angioscope (Class II - Special Controls, product code LYK).
Submitted by Applied Medical Resources (Launa Hills, US). The FDA issued a Cleared decision on February 10, 1995, 88 days after receiving the submission on November 14, 1994.
This device falls under the Cardiovascular FDA review panel. Regulated under 21 CFR 876.1500.
| 510(k) Number | K945591 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | November 14, 1994 |
| Decision Date | February 10, 1995 |
| Days to Decision | 88 days |
| Submission Type | Traditional |
| Review Panel | Cardiovascular (CV) |
| Summary | Summary PDF |
| Product Code | LYK — Angioscope |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 876.1500 |