ClearanceBrief
510(k) K940255 ยท NHK Resuscitator, Manual, Non Self-Inflating

HYPERINFLATION BAG SYSTEM

ApplicantNutec, Inc., Winfield IL, US
DecisionSubstantially Equivalent, Feb 17, 1994
ReceivedJan 19, 1994
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K940255

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.