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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: K101784
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Biosense Webster MobiCath Bi-Directional Guiding Sheath. Small Curve catalog no. D140010, Large Cur... 2 12/22/2012 FEI # 2183787
Greatbatch Medical
Biosense Webster MobiCath Bi-Directional Guiding Sheath. Small Curve catalog no. D140010, Large Cur... 2 10/24/2012 FEI # 2183787
Greatbatch Medical
CT3Plus (a.k.a. CT3PZ); Catalog number: 7300-0038/ 7300-0038-1. Dermatology: For use in dermat... 2 09/30/2016 FEI # 1000307100
New Star Lasers, Inc.
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