ClearanceBrief
510(k) K933232 ยท KDP Regulator, Vacuum

BOEHRINGER LABORATORIES SUCTION REGULATOR, MODIFIED

ApplicantBoehringer Laboratories, Norristown PA, US
DecisionSubstantially Equivalent, Mar 28, 1994
ReceivedJul 6, 1993
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K933232

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.