510(k) K010260 ยท HNO Keratome, Ac-Powered
HANSATOME MICROKERATOME
| Applicant | Bausch & Lomb, Inc., Irvine CA, US |
| Decision | Substantially Equivalent, Apr 27, 2001 |
| Received | Jan 29, 2001 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K010260
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.