Submission Details
| 510(k) Number | K022840 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | August 27, 2002 |
| Decision Date | November 01, 2002 |
| Days to Decision | 66 days |
| Submission Type | Traditional |
| Review Panel | Ophthalmic (OP) |
| Summary | Summary PDF |
K022840 is an FDA 510(k) clearance for the STEPHENS DISPOSABLE SCISSORS, a Scissors, Ophthalmic (Class I — General Controls, product code HNF), submitted by Stephens Instruments (Lexington, US). The FDA issued a Cleared decision on November 1, 2002, 66 days after receiving the submission on August 27, 2002. This device falls under the Ophthalmic review panel. Regulated under 21 CFR 886.4350.
| 510(k) Number | K022840 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | August 27, 2002 |
| Decision Date | November 01, 2002 |
| Days to Decision | 66 days |
| Submission Type | Traditional |
| Review Panel | Ophthalmic (OP) |
| Summary | Summary PDF |
| Product Code | HNF — Scissors, Ophthalmic |
| Device Class | Class I — General Controls |
| CFR Regulation | 21 CFR 886.4350 |