510(k) K232261 · LDF Electrode, Pacemaker, Temporary

TME Temporary Myocardial Electrode

Applicant	Osypka AG, Rheinfelden, DE
Decision	Substantially Equivalent, Apr 26, 2024
Received	Jul 31, 2023
Type	Traditional
FDA record	Open on fda.gov

Recalls that name K232261

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.