510(k) K014000 ยท HNO Keratome, Ac-Powered
VISTITOME 20-10 MICROKERATOME
| Applicant | Biovision AG, Irvine CA, US |
| Decision | Substantially Equivalent, Mar 11, 2002 |
| Received | Dec 4, 2001 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K014000
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.