ClearanceBrief
510(k) K896934 ยท BZQ Monitor, Breathing Frequency

KNIGHTWATCH SYSTEM

ApplicantCreatech Corp., Washington, D.C. DC, US
DecisionSubstantially Equivalent, Jun 25, 1990
ReceivedDec 13, 1989
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K896934

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.