ClearanceBrief
510(k) K251403 · FAS Electrode, Electrosurgical, Active, Urological

Dornier Bi-Polar Electrode BIP12CLM Bipolar 12° Medium Cutting Loop 24 Fr Electrode-Sterile, Single-Use BIP12CLL Bipolar 12° Large Cutting Loop 24 Fr Electrode-Sterile, Single-Use BIP30CLM Bipolar 30° Medium Cutting Loop 24 Fr Electrode-Sterile, Single-Use BIP30CLL Bipolar 30° Large Cutting Loop 24

ApplicantDornier Medtech America Inc (Dmta), Kennesaw GA, US
DecisionSubstantially Equivalent, Dec 5, 2025
ReceivedMay 6, 2025
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K251403

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.