Myelotec, Inc.
2 FDA 510(k) clearances · Recalling firm
| Record | Firm | Date |
|---|---|---|
| Myelotec Steerable Video Guided Catheter, 2.7mm, label insert for LB0013-1, LB0013-2, and recall (Z-0586-2008) | Myelotec, Inc. | 2008-04-10 |
| Myelotec Steerable Video Guided Catheter, 3.0mm, Label Insert contained in LB0020-0, LB002 recall (Z-0587-2008) | Myelotec, Inc. | 2008-04-10 |
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Every clearance here is in the API, with alerts when new ones post.