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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: K192482
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Elekta Unity, Image-Guided Radiation Therapy System 2 06/30/2020 Elekta, Inc.
Elekta Unity, Philips Marlin Software versions: R5.3.30, R5.3.31, R6.0.5331, R5.7.0, R5.7.1, R6.1.57... 2 06/08/2020 Elekta Limited
Elekta Unity, UDI 05060191071321, Image-guided radiation therapy system - Product Usage: is indicate... 2 06/05/2020 Elekta, Inc.
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