ClearanceBrief
510(k) K001030 ยท BZQ Monitor, Breathing Frequency

RESPIRATORY BELT SENSOR, MODEL 6000S; LIMB MOVEMENT SENSOR, MODEL 3000S

ApplicantDymedix, Inc., Stoughton WI, US
DecisionSubstantially Equivalent, May 11, 2000
ReceivedMar 30, 2000
TypeAbbreviated
FDA recordOpen on fda.gov

Recalls that name K001030

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.