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U.S. Department of Health and Human Services

Medical Device Recalls
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510(K) Number: K183456
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Ultrasonic pulsed doppler imaging system - Product Usage: intended for use by trained personnel (doc... 2 03/19/2021 Hitachi Medical Systems America Inc
Model L43K Intraoperative Probe-For the diagnostic ultrasound evaluation during robotic/non-robotic... 2 08/16/2021 Hitachi Healthcare Americas Corporation
Arietta 850 Ultrasound- Software Version: V1.0.0 through V4.1.3 2 11/02/2021 FujiFilm Healthcare Americas Corporation
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