The following data is part of a premarket notification filed by Bridgepoint Medical with the FDA for Bridgepoint Medical Crossboss Catheter, Model M-2000.
| Device ID | K091841 |
| 510k Number | K091841 |
| Device Name: | BRIDGEPOINT MEDICAL CROSSBOSS CATHETER, MODEL M-2000 |
| Classification | Catheter, Percutaneous |
| Applicant | BRIDGEPOINT MEDICAL 2800 CAMPUS DRIVE #50 Plymouth, MN 55441 |
| Contact | Jill Munsinger |
| Correspondent | Jill Munsinger BRIDGEPOINT MEDICAL 2800 CAMPUS DRIVE #50 Plymouth, MN 55441 |
| Product Code | DQY |
| CFR Regulation Number | 870.1250 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2009-06-22 |
| Decision Date | 2009-09-02 |
| Summary: | summary |