K880345 is an FDA 510(k) clearance for the CYSTOTOMES/KNIFES. This device is classified as a Cystotome (Class I - General Controls, product code HNY).
Submitted by Myocure, Inc. (Glendale, US). The FDA issued a Cleared decision on May 3, 1988, 98 days after receiving the submission on January 26, 1988.
This device falls under the Ophthalmic FDA review panel. Regulated under 21 CFR 886.4350.
| 510(k) Number | K880345 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | January 26, 1988 |
| Decision Date | May 03, 1988 |
| Days to Decision | 98 days |
| Submission Type | Traditional |
| Review Panel | Ophthalmic (OP) |
| Summary | — |
| Product Code | HNY — Cystotome |
| Device Class | Class I - General Controls |
| CFR Regulation | 21 CFR 886.4350 |