510(k) K030401 ยท HNO Keratome, Ac-Powered
DISPOSABLE M2-PE MICROKERATOME BLADES
| Applicant | Oasis Medical, Inc., Glendora CA, US |
| Decision | Substantially Equivalent, Jun 19, 2003 |
| Received | Feb 6, 2003 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K030401
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.