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