ClearanceBrief
510(k) K232980 ยท MQK Labware, Assisted Reproduction

SpermAlign Sperm Separation Device

ApplicantCytoswim, Ltd., Coventry, GB
DecisionSubstantially Equivalent, Mar 14, 2024
ReceivedSep 21, 2023
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K232980

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.