ClearanceBrief
510(k) K781158 ยท BZQ Monitor, Breathing Frequency

ALARM UNIT, BATTERY OPERATED

ApplicantThompson Respiration Products, Inc., Mchenry IL, US
DecisionSubstantially Equivalent, Dec 18, 1978
ReceivedJul 5, 1978
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K781158

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.