510(k) K103103 ยท GXZ Electrode, Needle
PRESSON ELECTRODE
| Applicant | Persyst Development Corp., Prescott AZ, US |
| Decision | Substantially Equivalent, Dec 8, 2011 |
| Received | Oct 20, 2010 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K103103
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.