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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 9 of 9 Results
510(K) Number: K151233
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Product Description
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FDA Recall
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Monaco Radiation Treatment Planning System. Used to make treatment plans for patients with prescr... 2 10/07/2015 FEI # 1037831
Elekta, Inc.
Monaco - Radiation Treatment Planning used to make treatment plans for patients with prescriptions ... 2 10/30/2015 FEI # 1037831
Elekta, Inc.
Monaco RTP System Product Usage: The Monaco system is used to make treatment plans for patients ... 2 06/02/2016 FEI # 1037831
Elekta, Inc.
Monaco RTP System The Monaco system is used to make treatment plans for patients with prescriptions... 2 10/13/2016 FEI # 1037831
Elekta, Inc.
Monaco RTP System; Used to make treatment plans for patients with prescriptions for external beam ra... 2 11/25/2016 FEI # 1037831
Elekta, Inc.
Monaco RTP System Product Usage: Used to make treatment plans for patients with prescriptions fo... 2 01/11/2017 FEI # 1037831
Elekta, Inc.
Monaco RTP System. Used to make treatment plans for patients with prescriptions for external beam... 2 01/18/2017 FEI # 1037831
Elekta, Inc.
Monaco RTP System, software versions 5.10 and 5.11, Radiation Treatment Planning System 2 07/27/2019 FEI # 1937649
Elekta Inc
Monaco RTP System. Used to make treatment plans for patients with prescriptions for external be... 2 03/08/2023 FEI # 1937649
Elekta Inc
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