ClearanceBrief
510(k) K070408 ยท DQA Oximeter

DURAMAX REUSABLE OXIMETRY SENSOR

ApplicantNellcor Puritan Bennett, Inc., Pleasanton CA, US
DecisionSubstantially Equivalent, May 25, 2007
ReceivedFeb 12, 2007
TypeAbbreviated
FDA recordOpen on fda.gov

Recalls that name K070408

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.