ClearanceBrief
510(k) K883304 ยท DRO Pacemaker, Cardiac, External Transcutaneous (Non-Invasive)

TRAID-EP, PLATE INPUT, W/PULSE BLANKING CIRCUITRY

ApplicantCardiotronics, Inc., West Carlsbad CA, US
DecisionSubstantially Equivalent, Nov 9, 1988
ReceivedAug 3, 1988
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K883304

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.