The following data is part of a premarket notification filed by Flowcardia, Inc. with the FDA for Crosser Lp System.
| Device ID | K080765 |
| 510k Number | K080765 |
| Device Name: | CROSSER LP SYSTEM |
| Classification | Wire, Guide, Catheter |
| Applicant | FLOWCARDIA, INC. 745 N. PASTORIA AVE. Sunnyvale, CA 94085 |
| Contact | Dustin Michaels |
| Correspondent | Dustin Michaels FLOWCARDIA, INC. 745 N. PASTORIA AVE. Sunnyvale, CA 94085 |
| Product Code | DQX |
| CFR Regulation Number | 870.1330 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2008-03-18 |
| Decision Date | 2008-06-20 |
| Summary: | summary |