510(k) K894911 ยท GXZ Electrode, Needle
SENSORY NEEDLE ELECTRODE DNE 111-115,116-117,118
| Applicant | Dantec Electronics, Inc., Allendale NJ, US |
| Decision | Substantially Equivalent, May 14, 1990 |
| Received | Aug 1, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K894911
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.