Submission Details
| 510(k) Number | K851754 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | April 25, 1985 |
| Decision Date | June 20, 1985 |
| Days to Decision | 56 days |
| Submission Type | Traditional |
| Review Panel | General & Plastic Surgery (SU) |
| Summary | — |
K851754 is an FDA 510(k) clearance for the 13-160 INCISION SCISSORS, TWO SIZES..
Submitted by Artiberia (San Antonio, US). The FDA issued a Cleared decision on June 20, 1985, 56 days after receiving the submission on April 25, 1985.
This device falls under the General & Plastic Surgery FDA review panel.
| 510(k) Number | K851754 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | April 25, 1985 |
| Decision Date | June 20, 1985 |
| Days to Decision | 56 days |
| Submission Type | Traditional |
| Review Panel | General & Plastic Surgery (SU) |
| Summary | — |
| Product Code | — |
| Device Class | — |