510(k) K982170 ยท FRN Pump, Infusion
FLUIDSENSE FLUID DELIVERY SYSTEM
| Applicant | Fluidsense Corp., Newburyport MA, US |
| Decision | Substantially Equivalent, Nov 30, 1998 |
| Received | Jun 19, 1998 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K982170
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.