ClearanceBrief
510(k) K920086 ยท LDD Dc-Defibrillator, Low-Energy, (Including Paddles)

SHOCK-PATCH ADULT DEFIBRILLATION PADS

ApplicantCardiotronics, Inc., West Carlsbad CA, US
DecisionSubstantially Equivalent, Feb 3, 1992
ReceivedJan 8, 1992
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K920086

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.