ClearanceBrief
510(k) K881087 ยท BTM Ventilator, Emergency, Manual (Resuscitator)

LIFEGUARD SINGLE USE MANUAL RESUSCITATORS

ApplicantLifeguard Medical Products, Inc., Indianapolis IN, US
DecisionSubstantially Equivalent, Apr 14, 1988
ReceivedMar 14, 1988
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K881087

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.