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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 6 of 6 Results
510(K) Number: K183037
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Elekta Monaco - Product Usage: used to make treatment plans for patients with prescriptions for exte... 2 09/24/2021 FEI # 1937649
Elekta Inc
Monaco RTP System, Software Builds 5.40.00, 5.40.01, 5.40.02, and 5.51.10 2 09/02/2021 FEI # 1937649
Elekta Inc
Elekta MONACO RTP Sytem, radiation treatment planning software system - Product Usage: The Monaco sy... 2 04/29/2020 FEI # 1937649
Elekta Inc
Monaco Radiation Treatment Planning System (RTP) System 2 12/12/2019 FEI # 1937649
Elekta Inc
Monaco RTP System, 5.40 Unity, radiation treatment planning system Product Usage: The Monaco sys... 2 09/25/2019 FEI # 1937649
Elekta Inc
Monaco Radiation Treatment Planning (RTP) System 2 02/27/2019 FEI # 1037831
Elekta, Inc.
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