ClearanceBrief
510(k) K802400 ยท FRN Pump, Infusion

MS 16 SYRINGE DRIVER

ApplicantPrinceton Medical Instruments, Inc., Mchenry IL, US
DecisionSubstantially Equivalent, Dec 16, 1980
ReceivedOct 2, 1980
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K802400

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.