ClearanceBrief
510(k) K102778 ยท JOY Device, Automated Cell-Locating

CELLAVISION DM1200 WITH THE BODY FLUID APPLICTION

ApplicantCellaVision AB, Fridley MN, US
DecisionSubstantially Equivalent, Sep 16, 2011
ReceivedSep 24, 2010
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K102778

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.