510(k) K821051 ยท HPX Lens, Contact (Polymethylmethacrylate)
LIQUIFILM WETTING SOLUTION
| Applicant | Allergan, Inc., Walker MI, US |
| Decision | Substantially Equivalent, May 13, 1982 |
| Received | Apr 15, 1982 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K821051
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.