ClearanceBrief
510(k) K900822 ยท DOX Fluorometer, Lead (Dedicated Instruments)

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ApplicantNational-Standard Medical Products, Gainesville FL, US
DecisionSubstantially Equivalent, Jul 17, 1990
ReceivedFeb 21, 1990
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K900822

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.