The following data is part of a premarket notification filed by Nxstage Medical, Inc. with the FDA for Nxstage Cartridge Express.
| Device ID | K014152 |
| 510k Number | K014152 |
| Device Name: | NXSTAGE CARTRIDGE EXPRESS |
| Classification | Dialyzer, High Permeability With Or Without Sealed Dialysate System |
| Applicant | NXSTAGE MEDICAL, INC. 439 SOUTH UNION ST. SUITE 501 Lawrence, MA 01843 |
| Contact | Norma Lemay |
| Correspondent | Norma Lemay NXSTAGE MEDICAL, INC. 439 SOUTH UNION ST. SUITE 501 Lawrence, MA 01843 |
| Product Code | KDI |
| CFR Regulation Number | 876.5860 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2001-12-18 |
| Decision Date | 2002-12-11 |
| Summary: | summary |