510(k) K030891 ยท HNO Keratome, Ac-Powered
SURGISTAR MICROKERATOME BLADE, MODEL NO. 2400-LSK
| Applicant | Surgistar, Inc., Carlsbad CA, US |
| Decision | Substantially Equivalent, Jun 17, 2003 |
| Received | Mar 21, 2003 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K030891
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.