ClearanceBrief
510(k) K782033 ยท DRL Tester, Defibrillator

CARDIAC CARE Q/C TEST KIT

ApplicantInstrumentation Laboratory CO, Mchenry IL, US
DecisionSubstantially Equivalent, Dec 15, 1978
ReceivedDec 6, 1978
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K782033

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.