Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K101784 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| 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. |
| Biosense Webster MobiCath Bi-Directional Guiding Sheath. Small Curve catalog no. D140010, Large Cur... | 2 | 10/24/2012 |
FEI # 2183787 Greatbatch Medical |
| Biosense Webster MobiCath Bi-Directional Guiding Sheath. Small Curve catalog no. D140010, Large Cur... | 2 | 12/22/2012 |
FEI # 2183787 Greatbatch Medical |
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