510(k) K021916 ยท FPA Set, Administration, Intravascular
HARMAC HUBER NEEDLE SAFETY DEVICE, H2984001
| Applicant | Harmac Medical Products, Inc., Buffalo NY, US |
| Decision | Substantially Equivalent, Aug 29, 2002 |
| Received | Jun 11, 2002 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K021916
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.