ClearanceBrief
510(k) K033688 ยท NRH System, Breath Measurement

MICRO H2 BREATH MONITORING DEVICE WITH HYDRA SOFTWARE UTILITY

ApplicantMicro Direct, Inc., Lewiston ME, US
DecisionSubstantially Equivalent, May 19, 2004
ReceivedNov 24, 2003
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K033688

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.