ClearanceBrief
510(k) K900349 ยท BTM Ventilator, Emergency, Manual (Resuscitator)

PURITAN BENNETT SINGLE PATIENT USE PEEP ADAPTER

ApplicantPuritan Bennett Corp., Overland Park KS, US
DecisionSubstantially Equivalent, May 1, 1990
ReceivedJan 24, 1990
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K900349

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.