510(k) K896544 ยท FRN Pump, Infusion
MD2 PERSONAL INFUSION SYSTEM
| Applicant | Norfolk Medical Products, Inc., Skokie IL, US |
| Decision | Substantially Equivalent, May 2, 1990 |
| Received | Nov 17, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K896544
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.