ClearanceBrief
510(k) K921666 ยท LDD Dc-Defibrillator, Low-Energy, (Including Paddles)

CARDIAC THERAPHY SYSTEM SCP 900

ApplicantPpg Hellige B.V., Lenexa KS, US
DecisionSubstantially Equivalent, Sep 23, 1993
ReceivedApr 7, 1992
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K921666

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.