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U.S. Department of Health and Human Services

Medical Device Recalls
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21 to 22 of 22 Results
510(K) Number: K955084
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BLACKMAX-NEURO LOW PRESSURE Product Usage: Pneumatic system 2 05/04/2017 FEI # 1045834
The Anspach Effort, Inc.
CONTRA ANGLE ATTACHMENT, BLACK MAX 2 05/04/2017 FEI # 1045834
The Anspach Effort, Inc.
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