ClearanceBrief
510(k) K010521 ยท JAF Monitor, Ultrasonic, Nonfetal

NICOLET VERSALAB

ApplicantNicolet Biomedical, Golden CO, US
DecisionSubstantially Equivalent, Mar 9, 2001
ReceivedFeb 22, 2001
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K010521

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.