510(k) K041206 ยท HNO Keratome, Ac-Powered
EPITOME SYSTEM
| Applicant | Gebauer Medizintechnik GmbH, Lexington MA, US |
| Decision | Substantially Equivalent, Sep 15, 2004 |
| Received | May 7, 2004 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K041206
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.