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U.S. Department of Health and Human Services

Medical Device Recalls
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1 result found
510(K) Number: K970530
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ANSPACH***REF-98-0056***Custom Device Autolube III modified with a swivel***Rx Only*** This devic... 2 06/25/2014 FEI # 1045834
The Anspach Effort, Inc.
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