Submission Details
| 510(k) Number | K001960 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | June 27, 2000 |
| Decision Date | August 28, 2000 |
| Days to Decision | 62 days |
| Submission Type | Traditional |
| Review Panel | Ophthalmic (OP) |
| Summary | Summary PDF |
K001960 is an FDA 510(k) clearance for the RIGID GAS PERMEABLE CONTACT LENS, a Lens, Contact (other Material) - Daily (Class II — Special Controls, product code HQD), submitted by Polymer Technology (Rochester, US). The FDA issued a Cleared decision on August 28, 2000, 62 days after receiving the submission on June 27, 2000. This device falls under the Ophthalmic review panel. Regulated under 21 CFR 886.5916.
| 510(k) Number | K001960 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | June 27, 2000 |
| Decision Date | August 28, 2000 |
| Days to Decision | 62 days |
| Submission Type | Traditional |
| Review Panel | Ophthalmic (OP) |
| Summary | Summary PDF |
| Product Code | HQD — Lens, Contact (other Material) - Daily |
| Device Class | Class II — Special Controls |
| CFR Regulation | 21 CFR 886.5916 |