Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K972846 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Kimberly-Clark RadiOpaque Radiofrequency Cannula, Gauge 22, Length 100 mm, Active Tip 10 mm, Distrib... | 2 | 01/28/2014 |
FEI # 1000015879 Kimberly-Clark Corporation |
| BMC RF Cannula Curved Sharp RadiOpaque, Non-Pyrogenic, Active Tip: 10mm, Gauge 16 Ga, Length: 100mm.... | 2 | 02/26/2013 |
FEI # 3000157372 Baylis Medical Company Inc. |
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