ClearanceBrief
510(k) K851092 ยท LDD Dc-Defibrillator, Low-Energy, (Including Paddles)

PORTABLE DEFIBRILLATOR/MONITOR ED 425

ApplicantHoneywell, Inc., Pleasantville NY, US
DecisionSubstantially Equivalent, Apr 10, 1985
ReceivedMar 19, 1985
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K851092

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.