ClearanceBrief
510(k) K014218 ยท DQA Oximeter

OSI MEDICAL DIGITAL DOLPHIN 3000 PULSE OXIMETER; DIGITAL DOLPHIN REUSABLE OPTICAL SENSOR, MODEL 210'

ApplicantDolphin Medical, Inc., Tampa FL, US
DecisionSubstantially Equivalent, Nov 7, 2002
ReceivedDec 21, 2001
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K014218

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.