510(k) K900054 ยท LRX Case, Contact Lens
KESTREL LENS CASE 1543-893S/P-1700-2611
| Applicant | Kestrel, Columbus IN, US |
| Decision | Substantially Equivalent, Jan 30, 1990 |
| Received | Jan 3, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K900054
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.