ClearanceBrief
510(k) K850740 ยท

SECHRIST VOLUME VENTILATOR MODIFICATION

ApplicantSechrist Industries, Inc., Anaheim CA, US
DecisionSubstantially Equivalent, Jul 29, 1985
ReceivedJan 28, 1985
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K850740

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.