The following data is part of a premarket notification filed by Gambro, Inc. with the FDA for Gambro Bicart System.
| Device ID | K873155 |
| 510k Number | K873155 |
| Device Name: | GAMBRO BICART SYSTEM |
| Classification | System, Dialysate Delivery, Single Patient |
| Applicant | GAMBRO, INC. 600 KNIGHTSBRIDGE PKWY. Lincolnshire, IL 60069 |
| Contact | Jeffrey Shideman,phd |
| Correspondent | Jeffrey Shideman,phd GAMBRO, INC. 600 KNIGHTSBRIDGE PKWY. Lincolnshire, IL 60069 |
| Product Code | FKP |
| CFR Regulation Number | 876.5820 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1987-08-10 |
| Decision Date | 1987-10-26 |