510(k) K972808 ยท HNO Keratome, Ac-Powered
HANSATOME MICROKERATOME
| Applicant | Chiron Vision Corp., Irvine CA, US |
| Decision | Substantially Equivalent, Oct 24, 1997 |
| Received | Jul 28, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K972808
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.