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FIBERNET EMBOLI PROTECTION DEVICE SYSTEM
 Request for Information Form |
 Contact Information
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| Company Name | LUMEN BIOMEDICAL, INC. |
| Address | 14505 21ST AVE. NORTH
SUITE 212 |
| City, State, Zip | PLYMOUTH, MN 55447 |
| Country | US |
| FDA Owner/Operator Phone | 763-577-9600 |
| 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 | PERCUTANEOUS CATHETER |
| FDA Proprietary Device Name | FIBERNET EMBOLI PROTECTION DEVICE SYSTEM |
| FDA Owner / Operator Number | 9074244 |
| FDA Owner / Operator Name | LUMEN BIOMEDICAL, INC. |
| FDA Establishment Registration Number | 3005522028 |
| FDA Registered Establishment Name | LUMEN BIOMEDICAL, INC. |
| FDA Operation Code(s) | |
| FDA Listing Date | 07-24-06 |
| FDA Listing Status Code | Active |
| Differentiation | N/A |
| Keywords | N/A |
| Description | N/A |
| Brochure | N/A |
| Product Website | N/A |
Competitors of LUMEN BIOMEDICAL, INC.
Our records indicate that the following medical device companies may manufacture a similar device.
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