K851800 is an FDA 510(k) clearance for the 69-100 TO 69-114 VARIOUS CUTICLE SCISSORS. This device is classified as a Scissors, Orthopedic, Surgical (Class I - General Controls, product code HRR).
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 Orthopedic FDA review panel. Regulated under 21 CFR 888.4540.
| 510(k) Number | K851800 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | April 25, 1985 |
| Decision Date | June 20, 1985 |
| Days to Decision | 56 days |
| Submission Type | Traditional |
| Review Panel | Orthopedic (OR) |
| Summary | — |
| Product Code | HRR — Scissors, Orthopedic, Surgical |
| Device Class | Class I - General Controls |
| CFR Regulation | 21 CFR 888.4540 |