ClearanceBrief
510(k) K834300 ยท JQP Calculator/Data Processing Module, For Clinical Use

HYBRITECH DATA STATION

ApplicantHybritech, Inc., Mchenry IL, US
DecisionSubstantially Equivalent, Feb 21, 1984
ReceivedDec 9, 1983
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K834300

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.