510(k) K030593 ยท LPL Lenses, Soft Contact, Daily Wear
FLEXLENS AND HARRISON POST REFRACTIVE SURGERY (BIOXIFILCON A), (HIOXIFILCON B), (ACOFILCON A), (ACOFILCON B) SOFT CONTAC
| Applicant | X-Cel Contacts, A Walman Co., Grand Junction CO, US |
| Decision | Substantially Equivalent, May 30, 2003 |
| Received | Feb 25, 2003 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K030593
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.