Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K102948 |
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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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TorFlex Transseptal Guiding Sheath ; Model numbers: TF8-32-63-45, TF8-32-63-55, TF8-32-63-90, TF8-32... | 2 | 05/21/2020 | Baylis Medical Company Inc. |
NRG RF Transseptal Kit; Model No.s : NTK-710-8545, NTK-710-8555, NTK-711-8545, NTK-711-8555, NTK-711... | 2 | 05/21/2020 | Baylis Medical Company Inc. |
Baylis Medical TorFlex Transseptal Guiding Sheath, Rx Only, non-pyrogenic, sterile. Product Usage... | 1 | 11/01/2013 | Baylis Medical Corp * |
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