Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K834352 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| DLP Left Heart Vent Catheters, 18 FR. Sterile, Rx Only | 2 | 09/22/2021 |
FEI # 1000116158 Medtronic Perfusion Systems |
| DLP Left Heart Vent Catheters, 16 FR. Sterile, Rx Only | 2 | 09/22/2021 |
FEI # 1000116158 Medtronic Perfusion Systems |
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