ClearanceBrief
510(k) K850200 ยท KDP Regulator, Vacuum

SUCTION REGULATOR 7700 SERIES

ApplicantBoehringer Laboratories, Norristown PA, US
DecisionSubstantially Equivalent, Mar 4, 1985
ReceivedJan 18, 1985
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K850200

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.