Medical Device Recalls
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1 to 4 of 4 Results
510(K) Number: K960200 |
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Product Description
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Recall
Class
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FDA Recall
Posting Date
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Recalling Firm
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| Arrow A Port with Attachable Silicone Rubber Catheters/10 Fr. Introducer Kit Implantable Vascular ... | 3 | 07/20/2004 | Arrow International Inc |
| Arrow Low Profile Port with Attachable Silicone Rubber Catheters/10 Fr. Introducer Kit Implantable... | 3 | 07/20/2004 | Arrow International Inc |
| Arrow Low Profile Port with Attachable Silicone Rubber Catheters/10 Fr. Introducer Kit Implantable (... | 3 | 07/20/2004 | Arrow International Inc |
| Arrow A Port with Attachable Silicone Rubber Catheters Implantable Vascular Access System (Product #... | 3 | 07/20/2004 | Arrow International Inc |
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