Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K163510 |
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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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Butterfly iQ Ultrasound System Auto Bladder Volume Tool-The Auto Bladder Volume Tool is a segmentati... | 2 | 03/17/2020 | Butterfly Network, Inc. |
Butterfly iQ Ultrasound System containing the Auto EF(Ejection Fraction) Tool REF/Model: 850-20003 ... | 2 | 03/17/2020 | Butterfly Network, Inc. |
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