Medical Device Recalls
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1 to 4 of 4 Results
510(K) Number: K782095 |
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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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NAMIC Manifolds. (1) NAMIC Angiographic MANIFOLD, Medium Pressure, REF 64038301, UPN H96564038... | 2 | 09/24/2021 | Medline Industries Inc |
NAMIC Stopcocks: (1) NAMIC STOPCOCK, 200 psi (14 bar), REF 70015002, UPN H965700150021, Three-way... | 2 | 09/24/2021 | Medline Industries Inc |
NAMIC Custom Angiographic Kit, Right Heart Kit, REF/Catalog # 60190254, Sterile, and bulk Non-Steril... | 2 | 11/09/2008 | Navilyst Medical |
''NAMIC Custom Angiographic Kit'' sold under the following labels: (1) Medical University of Sou... | 3 | 08/24/2005 | Boston Scientific Corp |
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