ClearanceBrief
510(k) K993205 ยท LDD Dc-Defibrillator, Low-Energy, (Including Paddles)

BOOKER BOX, MODEL PAD 5010

ApplicantTz Medical, Inc., Lake Oswego OR, US
DecisionSubstantially Equivalent, Jul 20, 2000
ReceivedSep 24, 1999
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K993205

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.