ClearanceBrief
510(k) K941404 ยท DRL Tester, Defibrillator

IMPULSE 4000 DEFIBRILLATOR/TRANSCUTANEOUS PACER ANALYZER

ApplicantHogan & Hartson, Washington DC, US
DecisionSubstantially Equivalent, Jun 29, 1994
ReceivedMar 23, 1994
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K941404

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.