510(k) K896685 ยท LRX Case, Contact Lens
BAUSCH & LOMB FREQUENT REPLACEMENT CASE SYSTEM
| Applicant | Bausch & Lomb, Inc., Rochester NY, US |
| Decision | Substantially Equivalent, Dec 26, 1989 |
| Received | Nov 28, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K896685
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.