510(k) K033182 ยท HNO Keratome, Ac-Powered
PRIZM KERATOME BLADE (B.D. MODEL), MODEL MK8530BD
| Applicant | Surgin Surgical Instrumentation, Inc., Tustin CA, US |
| Decision | Substantially Equivalent, Jan 30, 2004 |
| Received | Oct 1, 2003 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K033182
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.