ClearanceBrief
510(k) K020881 ยท FRN Pump, Infusion

MODIFICATION TO PERSONAL INFUSOR LOCAL PAIN MANAGEMENT PROCEDURAL KIT

ApplicantScience Incorporated, Burnsville MN, US
DecisionSubstantially Equivalent, Mar 27, 2002
ReceivedMar 18, 2002
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K020881

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.