Cordis Neurovascular, Inc.
3 FDA 510(k) clearances · Recalling firm
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| Record | Firm | Date |
|---|---|---|
| Cordis Neurovascular Pre-Shaped PROWLER Infusion Catheters. recall (Z-1482-06) | Cordis Neurovascular, Inc. | 2006-09-02 |
| Cordis Neurovascular Pre-Shaped Prowler Select Infusion Catheters. recall (Z-1483-06) | Cordis Neurovascular, Inc. | 2006-09-02 |
| Product is labeled as Cordis Pre-shaped Prowler Plus MP Infusion Catheter (3 F proximal OD recall (Z-0018-04) | Cordis Neurovascular, Inc. | 2003-10-15 |
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Every clearance here is in the API, with alerts when new ones post.