Medical Device Recalls
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1 result found
510(K) Number: K941252 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Blood pressure (BP) circuit of the ANSAR ANX-3.0 Autonomic Monitor system. The ANX 3.0 system is... | 2 | 08/19/2014 |
FEI # 3000210032 Ansar Group, Inc. Dba Ansar Medical Technologies, Inc |
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