K821275 is an FDA 510(k) clearance for the MAYO SCISSOR STRAIGHT 5 1/2. This device is classified as a Scissors, Surgical Tissue, Dental (Class I - General Controls, product code EGN).
Submitted by Conphar, Inc. (Walker, US). The FDA issued a Cleared decision on May 28, 1982, 25 days after receiving the submission on May 3, 1982.
This device falls under the Dental FDA review panel. Regulated under 21 CFR 872.4565.
| 510(k) Number | K821275 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | May 03, 1982 |
| Decision Date | May 28, 1982 |
| Days to Decision | 25 days |
| Submission Type | Traditional |
| Review Panel | Dental (DE) |
| Summary | — |
| Product Code | EGN — Scissors, Surgical Tissue, Dental |
| Device Class | Class I - General Controls |
| CFR Regulation | 21 CFR 872.4565 |