510(k) K000233 ยท HQD Lens, Contact (Other Material) - Daily
MENICON SF-P
| Applicant | Menicon Co, Ltd., Wilmington MA, US |
| Decision | Substantially Equivalent, May 19, 2000 |
| Received | Jan 27, 2000 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K000233
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.