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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K183456
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Model L43K Intraoperative Probe-For the diagnostic ultrasound evaluation during robotic/non-robotic... 2 08/16/2021 FEI # 1528028
Hitachi Healthcare Americas Corporation
Ultrasonic pulsed doppler imaging system - Product Usage: intended for use by trained personnel (doc... 2 03/19/2021 FEI # 1528028
Hitachi Medical Systems America Inc
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