ClearanceBrief
510(k) K002623 ยท MQL Media, Reproductive

PURESPERM 40 AND PURESPERM 80

ApplicantNidacon International AB, Deer Field IL, US
DecisionSubstantially Equivalent, Nov 20, 2000
ReceivedAug 23, 2000
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K002623

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.