Medical Device Recalls
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1 result found
510(K) Number: K073326 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| NRG Transseptal Needle and NRG RF Transseptal Kit. Model/Catalogue Numbers: NRG-56-32-C0, NRG-71-... | 2 | 11/10/2016 |
FEI # 3005241199 Baylis Medical Corp * |
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