510(k) K936029 ยท FMI Needle, Hypodermic, Single Lumen
NON-CORNING (HUBER) NEEDLE
| Applicant | Therex Corp., Walpole MA, US |
| Decision | Substantially Equivalent, Feb 4, 1994 |
| Received | Dec 17, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K936029
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.