K142641 is an FDA 510(k) clearance for the Intelliwave4. This device is classified as a Lenses, Soft Contact, Daily Wear (Class II - Special Controls, product code LPL).
Submitted by Art Optical Contact Lens, Inc. (Walker, US). The FDA issued a Cleared decision on January 12, 2015, 117 days after receiving the submission on September 17, 2014.
This device falls under the Ophthalmic FDA review panel. Regulated under 21 CFR 886.5925.
| 510(k) Number | K142641 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | September 17, 2014 |
| Decision Date | January 12, 2015 |
| Days to Decision | 117 days |
| Submission Type | Traditional |
| Review Panel | Ophthalmic (OP) |
| Summary | Summary PDF |
| Product Code | LPL - Lenses, Soft Contact, Daily Wear |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 886.5925 |