ClearanceBrief
510(k) K242759 ยท HAE Rongeur, Manual

Geister K-Rex rongeurs

ApplicantGeister Medizin Technik GmbH, Tuttlingen, DE
DecisionSubstantially Equivalent, Jun 6, 2025
ReceivedSep 12, 2024
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K242759

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.