510(k) K960591 ยท IKT Electrode, Needle, Diagnostic Electromyograph
RE-USABLE BIPOLAR CONCENTRIC NEEDLE(237-XXX-24,237-XXX-24STP, 237-XXX-24TP,237-XXX-24STP
| Applicant | Chalgren Enterprises, Inc., Gilroy CA, US |
| Decision | Substantially Equivalent, Jun 13, 1996 |
| Received | Feb 12, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K960591
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.