Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K163082 |
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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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MyLab Ultrasound System; Models 6100, 6150, 6200, 6250; Probes: BL433, C 18, CA541, EC1123, EC123, I... | 2 | 03/20/2018 | ESAOTE S.P.A. |
MyLab Ultrasound System; Models 6100, 6150, 6200, 6250; PA023E Probe 7.5/10 | 2 | 03/20/2018 | ESAOTE S.P.A. |
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