ClearanceBrief
510(k) K020102 ยท BZG Spirometer, Diagnostic

IQTEQ SPIROMETER

ApplicantIqteq Development, Cape Town, Western Cape, ZA
DecisionSubstantially Equivalent, Mar 21, 2003
ReceivedJan 11, 2002
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K020102

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.