ClearanceBrief
510(k) K000814 ยท DQA Oximeter

FINGER PULSE METER

ApplicantBhs Intl., Inc., Crofton MD, US
DecisionSubstantially Equivalent, Mar 29, 2001
ReceivedMar 13, 2000
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K000814

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.