510(k) K000247 ยท LPN Accessories, Soft Lens Products
BAUSCH & LOMB RENU 1 STEP DAILY PROTEIN REMOVER
| Applicant | Bausch & Lomb, Inc., Rochester NY, US |
| Decision | Substantially Equivalent, Apr 20, 2000 |
| Received | Jan 27, 2000 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K000247
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.