K890825 is an FDA 510(k) clearance for the JUMPER PACK #203. This device is classified as a Unit, Phacofragmentation (Class II - Special Controls, product code HQC).
Submitted by O.R. Specialties, Inc. (Tuscaloosa, US). The FDA issued a Cleared decision on May 26, 1989, 98 days after receiving the submission on February 17, 1989.
This device falls under the Ophthalmic FDA review panel. Regulated under 21 CFR 886.4670.
| 510(k) Number | K890825 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | February 17, 1989 |
| Decision Date | May 26, 1989 |
| Days to Decision | 98 days |
| Submission Type | Traditional |
| Review Panel | Ophthalmic (OP) |
| Summary | — |
| Product Code | HQC — Unit, Phacofragmentation |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 886.4670 |