ClearanceBrief
510(k) K033101 ยท MQL Media, Reproductive

G-PGD

ApplicantVitrolife Sweden AB, Washington DC, US
DecisionSubstantially Equivalent, May 7, 2004
ReceivedSep 29, 2003
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K033101

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.