ClearanceBrief
510(k) K010009 ยท BZH Meter, Peak Flow, Spirometry

KOKO PEAK KP; KOKO PEAK KP+

ApplicantPds Healthcare Products, Inc., Louisville CO, US
DecisionSubstantially Equivalent, Jun 1, 2001
ReceivedJan 2, 2001
TypeAbbreviated
FDA recordOpen on fda.gov

Recalls that name K010009

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.