Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K073297 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| GE HEALTHCARE LOGIQ P6 Premium TruScan(TM) Imagining Technology: (a) Model BT09 (b) Model BT07 Pr... | 2 | 01/30/2019 |
FEI # 2126677 GE Healthcare, LLC |
| GE LOGIQ P6 Ultrasound System. The device is intended for use by a qualified physician for the ev... | 2 | 01/21/2012 |
FEI # 2126677 GE Healthcare, LLC |
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