510(k) K904961 ยท HQT Shell, Scleral
ARTIFICIAL SCLERAL SHELL
| Applicant | Midwest Eye Laboratories, Inc., Minneapolis MN, US |
| Decision | Substantially Equivalent, Aug 30, 1991 |
| Received | Nov 5, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K904961
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.