ClearanceBrief
510(k) K240002 · MQK Labware, Assisted Reproduction

G-Vitri™ Vitrification Straw

ApplicantGimbo Medical Technology Shenzhen Co., Ltd., Shenzhen, CN
DecisionSubstantially Equivalent, Jun 14, 2024
ReceivedJan 2, 2024
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K240002

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.