ClearanceBrief
510(k) K100773 ยท BZQ Monitor, Breathing Frequency

KAI SPOT MODEL KMS 200

ApplicantKai Medical, Inc., Honolulu HI, US
DecisionSubstantially Equivalent, Jun 23, 2010
ReceivedMar 18, 2010
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K100773

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.