510(k) K001144 ยท HNO Keratome, Ac-Powered
ULTRAEDGE KERATOME BLADE, MODEL 374803 - ACS
| Applicant | Lasersight Technologies, Inc., Winter Park FL, US |
| Decision | Substantially Equivalent, May 5, 2000 |
| Received | Apr 10, 2000 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K001144
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.