Submission Details
| 510(k) Number | K821290 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | May 04, 1982 |
| Decision Date | May 28, 1982 |
| Days to Decision | 24 days |
| Submission Type | Traditional |
| Review Panel | Ophthalmic (OP) |
| Summary | — |
K821290 is an FDA 510(k) clearance for the LITTAUER SCISSORS 5 1/2, a Scissors, Ophthalmic (Class I — General Controls, product code HNF), submitted by Conphar, Inc. (Mchenry, US). The FDA issued a Cleared decision on May 28, 1982, 24 days after receiving the submission on May 4, 1982. This device falls under the Ophthalmic review panel. Regulated under 21 CFR 886.4350.
| 510(k) Number | K821290 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | May 04, 1982 |
| Decision Date | May 28, 1982 |
| Days to Decision | 24 days |
| Submission Type | Traditional |
| Review Panel | Ophthalmic (OP) |
| Summary | — |
| Product Code | HNF — Scissors, Ophthalmic |
| Device Class | Class I — General Controls |
| CFR Regulation | 21 CFR 886.4350 |