ClearanceBrief
510(k) K212333 ยท IYN System, Imaging, Pulsed Doppler, Ultrasonic

Aplio i900/i800/i700 Diagnostic Ultrasound System, Software V6.5

ApplicantCanon Medical Systems Corporation, Otawara-Shi, JP
DecisionSubstantially Equivalent, Jan 24, 2022
ReceivedJul 27, 2021
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K212333

DateFirm and productCodeLinked 510(k)
Nov 8, 2022Canon Medical System, USA, INC.
Canon Aplio ultrasound system, Model: Aplio i900 TUS-AI900, Aplio i800 TUS-AI800, Aplio i700 TUS-AI700, Aplio a550 CUS-AA550, Aplio a450 CUS-AA450
Open, Classified
IYNNone listed

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