K921135 is an FDA 510(k) clearance for the IOLAB POWER I.V. POLE. This device is classified as a Unit, Phacofragmentation (Class II - Special Controls, product code HQC).
Submitted by Site Microsurgical Systems, Inc. (Horsham, US). The FDA issued a Cleared decision on June 3, 1992, 85 days after receiving the submission on March 10, 1992.
This device falls under the Ophthalmic FDA review panel. Regulated under 21 CFR 886.4670.
| 510(k) Number | K921135 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | March 10, 1992 |
| Decision Date | June 03, 1992 |
| Days to Decision | 85 days |
| Submission Type | Traditional |
| Review Panel | Ophthalmic (OP) |
| Summary | Statement |
| Product Code | HQC — Unit, Phacofragmentation |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 886.4670 |