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ANGIOGUARD EMBOLI CAPTURE GUIDEWIRE
 Request for Information Form |
 Contact Information
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| Company Name | CORDIS CORPORATION |
| Address | 14201 N.W. 60TH AVE. |
| City, State, Zip | MIAMI LAKES, FL 33014 |
| Country | US |
| FDA Owner/Operator Phone | 786-313-2000 |
| FDA Medical Specialty Code | CV - Cardiovascular |
| FDA Product Code | NTE |
| FDA Classification Name | CATHETER, CAROTID, TEMPORARY, FOR EMBOLIZATION CAPTURE |
| FDA Device Classification Code | Standards |
| FDA Regulation Number | 870.1250 |
| FDA Common Generic Name | STERILE, EMBOLI CAPTURE GUIDEWIRE |
| FDA Proprietary Device Name | ANGIOGUARD EMBOLI CAPTURE GUIDEWIRE |
| FDA Owner / Operator Number | 1016427 |
| FDA Owner / Operator Name | CORDIS CORPORATION |
| FDA Establishment Registration Number | 1016427 |
| FDA Registered Establishment Name | CORDIS CORPORATION |
| FDA Operation Code(s) |
MM - Manufacturer |
| FDA Listing Date | 09-26-06 |
| FDA Listing Status Code | Active |
| Differentiation | N/A |
| Keywords | N/A |
| Description | N/A |
| Brochure | N/A |
| Product Website | N/A |
Competitors of CORDIS CORPORATION
Our records indicate that the following medical device companies may manufacture a similar device.
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