ClearanceBrief
510(k) K010482 ยท JOP Transducer, Ultrasonic

ECHOFLOW PORTABLE DOPPLER BLOOD FLOW MEASUREMENT SYSTEM; MODEL PEF-1

ApplicantEchocath, Inc., Monmouth Junction NJ, US
DecisionSubstantially Equivalent, Mar 20, 2001
ReceivedFeb 20, 2001
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K010482

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.