ClearanceBrief
510(k) K852746 ยท JOQ Generator, Pulse, Pacemaker, External Programmable (For Electrophysiological Studies Only)

EXTERNAL PACEMAKER TELECTRONICS TE200

ApplicantSeamed Corp., Redmond WA, US
DecisionSubstantially Equivalent, Sep 12, 1985
ReceivedJun 27, 1985
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K852746

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.