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U.S. Department of Health and Human Services

Medical Device Recalls
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510(K) Number: K962613
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Treatment applicator for Gulmay Medical 150 or Xstrahl 150 superficial X-ray therapy system 2 12/16/2021 FEI # 3004561814
Xstrahl Limited
Concerto User Interface Software provided with the following systems: (1) Xstrahl 100 Electronic ... 2 10/26/2021 FEI # 3004561814
Xstrahl Limited
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