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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K853095
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FDA Recall
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Boehringer Suction Regulator Model number 3704 2 11/17/2005 Boehringer Laboratories, Inc.
Boehringer Suction Regulator Model number 3704D3 2 11/17/2005 Boehringer Laboratories, Inc.
Boehringer Suction Regulator Model number 3714 2 11/17/2005 Boehringer Laboratories, Inc.
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