510(k) K052290 ยท LPL Lenses, Soft Contact, Daily Wear
AQUASOFT ALL-DAY & ALL-DAY T (HIOXIFILCON A) DAILY WEAR CONTACT LENS
| Applicant | Clearlab Pte , Ltd., Grand Junction CO, US |
| Decision | Substantially Equivalent, May 15, 2006 |
| Received | Aug 23, 2005 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K052290
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.