ClearanceBrief
510(k) K240434 ยท HHK Curette, Suction, Endometrial (And Accessories)

RELIEEV Suction Curette (Flexible 3.0/ Standard 3.6)

ApplicantLi Medical Corporation , Ltd., New Taipei City, TW
DecisionSubstantially Equivalent, Sep 25, 2024
ReceivedFeb 14, 2024
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K240434

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.