510(k) K960405 ยท MIA Needle, Spinal, Short Term
SPINAL NEEDLE
| Applicant | Promex, Inc., Indianapolis IN, US |
| Decision | Substantially Equivalent, Feb 28, 1996 |
| Received | Jan 29, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K960405
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.