Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K201130 |
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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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Diagnostic Ultrasound System, ACUSON Juniper, UDI: (01)04056869152059, Model: 11335791, Rx, CE ... | 2 | 03/11/2022 | Siemens Medical Solutions USA, Inc. |
ACUSON Juniper Diagnostic Ultrasound System | 2 | 09/14/2021 | Siemens Medical Solutions USA, Inc. |
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