Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K120691 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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13.5 mm x 60 mm BrainPath Sheath The NICO BrainPath is a family of products that consists of mult... | 2 | 08/13/2012 | Nico Corp. |
13.5 mm x 50 mm BrainPath Sheath The NICO BrainPath is a family of products that consists of mult... | 2 | 08/13/2012 | Nico Corp. |
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