ClearanceBrief
510(k) K950483 ยท DRO Pacemaker, Cardiac, External Transcutaneous (Non-Invasive)

HEWLETT PACKARD M2475B CODEMASTER 100 DEFIBRILLATOR/MONITOR

ApplicantHewlett-Packard Co., Mcminnville OR, US
DecisionSubstantially Equivalent, May 22, 1995
ReceivedFeb 3, 1995
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K950483

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.