ClearanceBrief
510(k) K850246 ยท

MASTER KIT A

ApplicantPro-Lab, Inc., Birmingham AL, US
DecisionSubstantially Equivalent, Apr 9, 1985
ReceivedJan 22, 1985
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K850246

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.