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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 10 of 37 Results
510(K) Number: K854714
 
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American Surgical Ultracot 9 mm x 50 mm (Glassine) Ref Number: 23-07G Product Usage: Neurosurgic... 2 05/26/2016 FEI # 1221144
American Surgical Company
American Surgical Ultracot 70 mm x 10090 mm Ref Number: 23-24 Product Usage: Neurosurgical and N... 2 05/26/2016 FEI # 1221144
American Surgical Company
American Surgical Ultracot 6 mm x 50 mm Ref Number: 23-06 Product Usage: Neurosurgical and Nonne... 2 05/26/2016 FEI # 1221144
American Surgical Company
American Surgical Ultracot 5 mm x 8 mm (Glassine) Ref Number: 23-01G Product Usage: Neurosurgical... 2 05/26/2016 FEI # 1221144
American Surgical Company
American Surgical Ultracot 5 mm x 8 mm Ref Number: 23-01 Product Usage: Neurosurgical and Nonneu... 2 05/26/2016 FEI # 1221144
American Surgical Company
American Surgical Ultracot 5 mm x 13 mm (Glassine) Ref Number: 23-02G Product Usage: Neurosurgica... 2 05/26/2016 FEI # 1221144
American Surgical Company
American Surgical Ultracot 30 mm x 70 mm (Glassine) Ref Number: 23-10G Product Usage: Neurosurgic... 2 05/26/2016 FEI # 1221144
American Surgical Company
American Surgical Ultracot 30 mm x 70 mm Ref Number: 23-10 Product Usage: Neurosurgical and No... 2 05/26/2016 FEI # 1221144
American Surgical Company
American Surgical Ultracot 20 mm x 60 mm (Glassine) Ref Number: 23-09G Product Usage: Neurosurgic... 2 05/26/2016 FEI # 1221144
American Surgical Company
American Surgical Ultracot 20 mm x 60 mm Ref Number: 23-09 Product Usage: Neurosurgical and Nonn... 2 05/26/2016 FEI # 1221144
American Surgical Company
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