K761253 is an FDA 510(k) clearance for the CYCLODIALYSIS SPAT. 15MM BLADE TITANIUM. This device is classified as a Spatula, Ophthalmic (Class I - General Controls, product code HND).
Submitted by Edward Weck, Inc. (Mchenry, US). The FDA issued a Cleared decision on December 16, 1976, 3 days after receiving the submission on December 13, 1976.
This device falls under the Ophthalmic FDA review panel. Regulated under 21 CFR 886.4350.
| 510(k) Number | K761253 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | December 13, 1976 |
| Decision Date | December 16, 1976 |
| Days to Decision | 3 days |
| Submission Type | Traditional |
| Review Panel | Ophthalmic (OP) |
| Summary | — |
| Product Code | HND — Spatula, Ophthalmic |
| Device Class | Class I - General Controls |
| CFR Regulation | 21 CFR 886.4350 |