510(k) K032242 ยท GES Blade, Scalpel
PERSONNA PLUS SAFETY SCALPEL SYSTEM
| Applicant | Omi Manufacturing Pty., Ltd., Deer Field IL, US |
| Decision | Substantially Equivalent, Sep 23, 2003 |
| Received | Jul 21, 2003 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K032242
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.