510(k) K072102 ยท HNO Keratome, Ac-Powered
EPIVISION SL SYSTEM
| Applicant | Gebauer Medizintechnik GmbH, Lexington MA, US |
| Decision | Substantially Equivalent, Jan 16, 2009 |
| Received | Jul 31, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K072102
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.