510(k) K990227 ยท HNO Keratome, Ac-Powered
ULTRASHAPER KERATOME
| Applicant | Lasersight Technologies, Inc., Winter Park FL, US |
| Decision | Substantially Equivalent, Jan 31, 2000 |
| Received | Jan 25, 1999 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K990227
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.