ClearanceBrief
510(k) K981726 ยท NHJ Device, Positive Pressure Breathing, Intermittent

PERCUSSIVETECH HF, MODEL 2001

ApplicantVortran Medical Technology 1, Inc., Sacramento CA, US
DecisionSubstantially Equivalent, Sep 17, 1998
ReceivedMay 15, 1998
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K981726

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.