ClearanceBrief
510(k) K102579 ยท MWI Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)

HYPERQ AD-100 SYSTEM

ApplicantBiological Signal Processing, Ltd., Somerset MA, US
DecisionSubstantially Equivalent, Dec 2, 2010
ReceivedSep 8, 2010
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K102579

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.