510(k) K033457 ยท HNO Keratome, Ac-Powered
M2 COMPATIBLE MICROKERATOME BLADE
| Applicant | Micro Specialties, Inc., Milford CT, US |
| Decision | Substantially Equivalent, May 25, 2004 |
| Received | Oct 30, 2003 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K033457
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.