510(k) K992978 ยท HNO Keratome, Ac-Powered
RICROKERATOME BLADE
| Applicant | Surgistar, Inc., Carlsbad CA, US |
| Decision | Substantially Equivalent, Nov 16, 1999 |
| Received | Sep 3, 1999 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K992978
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.