ClearanceBrief
510(k) K800364 ยท DKX Thin Layer Chromatography, Barbiturate

ULTRASONIC DIAGNOSTIC SYSTEM, MOD. 202

ApplicantHoffrel Instruments, Inc., Mchenry IL, US
DecisionSubstantially Equivalent, Mar 12, 1980
ReceivedFeb 20, 1980
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K800364

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.