ClearanceBrief
510(k) K242089 ยท MQL Media, Reproductive

Vitrification Freeze Kit (RFD-0101) Vitrification Thaw Kit (RFD-0201, RFD-0202)

ApplicantJiangsu Ruifuda Medical Device Co., Ltd., Lianyungang, CN
DecisionSubstantially Equivalent, Apr 10, 2025
ReceivedJul 17, 2024
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K242089

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.