ClearanceBrief
510(k) K951901 ยท JEH Plethysmograph, Volume

MASTERSCREEN PFT BODY

ApplicantErich Jaeger GmbH & Co. KG, Hoechberg, DE
DecisionSubstantially Equivalent, Jul 31, 1995
ReceivedApr 24, 1995
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K951901

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.