Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K980734 |
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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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Myelotec Video Guided Catheters, REF 2010 3.0 mm OD x 30 Cm Working Length, Two 1.3mm Working Chann... | 2 | 07/28/2017 | Myelotec, Inc. |
Myelotec® Steerable Video Guided Catheter, 3.0mm, Label Insert contained in LB0020-0, LB0020-1, LB00... | 2 | 04/10/2008 | Myelotec, Inc. |
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