Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K102043 |
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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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UltraStream Chronic Hemodialysis Catheter Standard Kit; Model Number 32101524 (24 cm), 32101528 (28c... | 2 | 09/24/2014 | Argon Medical Devices, Inc |
UltraStream Peel Away Kit; Model Numbers 32401524 (24 cm), 32401528 (28cm), 32401532 (32 cm), and 32... | 2 | 09/24/2014 | Argon Medical Devices, Inc |
UltraStream Exchange Kit Model Numbers 32001524 (24 cm), 32001528 (28cm), 32001532 (32 cm), and 3200... | 2 | 09/24/2014 | Argon Medical Devices, Inc |
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