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U.S. Department of Health and Human Services

Medical Device Recalls

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1 to 3 of 3 Results
510(K) Number: K092438
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Product Description
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FDA Recall
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Ziehm Solo, Mobile C-arm for Mobile Fluoroscopic Imaging 2 08/25/2016 Ziehm Imaging Inc
Ziehm Solo C-Arm Interventional Fluoroscopic X-Ray System. Mobile Fluoroscopic Imaging 2 12/24/2013 Ziehm Imaging Inc
Double foot switch, type KF 2 1S/1 S-MED-AP, manufactured by the company Seute Schaltgerate. GmbH & ... 2 04/16/2012 Ziehm Imaging Inc