ClearanceBrief
510(k) K083879 ยท BZG Spirometer, Diagnostic

INNOCOR ERGOSPIROMETRY SYSTEM (INN00010), THE BASIC INNOCOR INCLUDING BREATH-BY-BREATH SYSTEM (INN00400), NIBP(INN00500)

ApplicantInnovision A/S, Lake Bluff IL, US
DecisionSubstantially Equivalent, Feb 23, 2009
ReceivedDec 29, 2008
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K083879

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.