510(k) K980924 ยท HNO Keratome, Ac-Powered
PLANCON MICROLAMELLAR KERATOME EVOLUTION
| Applicant | Plancon Instruments, Antony, FR |
| Decision | Substantially Equivalent, Apr 15, 1998 |
| Received | Mar 11, 1998 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K980924
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.