ClearanceBrief
510(k) K991410 ยท DQA Oximeter

3402 HANDHELD PULSE OXIMETER

ApplicantBci Intl., Inc., Waukesha WI, US
DecisionSubstantially Equivalent, Jun 9, 1999
ReceivedApr 22, 1999
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K991410

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.