510(k) K123915 ยท GXY Electrode, Cutaneous
DE48-PLUS
| Applicant | Grass Technologies, an Astro-Med, Inc. Product Gro, Rockland MA, US |
| Decision | Substantially Equivalent, Apr 24, 2013 |
| Received | Dec 19, 2012 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K123915
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.