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Cordis Neurovascular, Inc.

3 FDA 510(k) clearances · Recalling firm

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RecordFirmDate
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.