ClearanceBrief
510(k) K050601 ยท DPW Flowmeter, Blood, Cardiovascular

SMARTDOP 45 VASCULAR DOPPLER

ApplicantKoven Technology, Inc., Houston TX, US
DecisionSubstantially Equivalent, Apr 15, 2005
ReceivedMar 9, 2005
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K050601

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.