Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K223531 |
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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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CARESCAPE Canvas 1000, Model Numbers: a) 5865770; b) 5865770-01040169; c) 5865770-01054142; d) ... | 2 | 06/21/2024 | GE Healthcare Finland Oy |
CARESCAPE Canvas Smart Display, Model Numbers: a) 5700023, b) 5700023-02, c) 5939590-102; monit... | 2 | 06/21/2024 | GE Healthcare Finland Oy |
F2-01 Frame, physiological patient monitor (with arrhythmia detection or alarms) | 2 | 09/29/2023 | GE Medical Systems China Co., Ltd. |
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