510(k) K003582 ยท FRN Pump, Infusion
FLUIDSENSE FLUID DELIVERY SYSTEM MODEL FS-01
| Applicant | Fluidsense Corp., Newburyport MA, US |
| Decision | Substantially Equivalent, Dec 5, 2000 |
| Received | Nov 20, 2000 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K003582
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.