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U.S. Department of Health and Human Services

Medical Device Recalls
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510(K) Number: K911732
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Labeling is as follows: Product Labeling: ''***Argon Medical Devices***CUSTOM MANIFOLD KIT***R... 2 08/03/2005 Argon Medical Devices, Inc
Product consists of a syringe used to inject fluids during an angiographic procedure for fluoroscopi... 2 08/03/2005 Argon Medical Devices, Inc
Product consists of a syringe used to inject fluids during an angiographic procedure for fluoroscopi... 2 08/03/2005 Argon Medical Devices, Inc
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