510(k) K974004 ยท HNO Keratome, Ac-Powered
AUTOMATED DISPOSABLE KERATOME (ADK)
| Applicant | Lasersight Technologies, Inc., Orlando FL, US |
| Decision | Substantially Equivalent, Jan 8, 1998 |
| Received | Oct 21, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K974004
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.