510(k) K002140 ยท MRC Products, Contact Lens Care, Rigid Gas Permeable
MENICON PROGENT REMOVER
| Applicant | Menicon Co, Ltd., Wilmington MA, US |
| Decision | Substantially Equivalent, Oct 10, 2000 |
| Received | Jul 17, 2000 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K002140
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.