Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K810368 |
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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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| Cook Salle Intraoperative Pyeloplasty Stent Set PRODUCT/CATALOG NUMBER/GPN: 4.0 Fr - SIPSF-04001... | 2 | 05/17/2019 | Cook Inc. |
| Percutaneous Malecot Nephrostomy Set, Global Product No. G16714 G19107 G19108 | 2 | 02/04/2020 | Cook Inc. |
| Percutaneous Pigtail Nephrostomy Set , Global Product No. G14094 G14095 G14899 G14329 | 2 | 02/04/2020 | Cook Inc. |
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