ClearanceBrief
510(k) K142054 ยท IYO System, Imaging, Pulsed Echo, Ultrasonic

IMACOR ZURA EVO IMAGING SYSTEM

ApplicantImacor, Inc., Garden City NY, US
DecisionSubstantially Equivalent, Sep 29, 2014
ReceivedJul 29, 2014
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K142054

DateFirm and productCodeLinked 510(k)
Oct 25, 2024ImaCor Inc.
ClariTEE Probe- Miniature transesophageal echo ultrasound probe for use with ImaCor ultrasound diagnostic platforms. Model/Catalog Number: CLT-010, CLT-010-1
Open, Classified
ITXNone listed

Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.