K842979 is an FDA 510(k) clearance for the CAVITRON/KELMAN PHACO-EMULSIFIER ASPIRA. This device is classified as a Unit, Phacofragmentation (Class II - Special Controls, product code HQC).
Submitted by CooperVision, Inc. (Irvine, US). The FDA issued a Cleared decision on November 27, 1984, 120 days after receiving the submission on July 30, 1984.
This device falls under the Ophthalmic FDA review panel. Regulated under 21 CFR 886.4670.
| 510(k) Number | K842979 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | July 30, 1984 |
| Decision Date | November 27, 1984 |
| Days to Decision | 120 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 |