ClearanceBrief
510(k) K981725 ยท BZQ Monitor, Breathing Frequency

OPTOVENT RESPIRATORY MONITOR MODEL NUMBER RR 9700

ApplicantOptovent, Inc., Fort Lee NJ, US
DecisionSubstantially Equivalent, Feb 2, 1999
ReceivedMay 15, 1998
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K981725

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.