The following data is part of a premarket notification filed by Renal Solutions, Inc. with the FDA for 2008 Hemodialysis Sorbent System.
| Device ID | K123835 |
| 510k Number | K123835 |
| Device Name: | 2008 HEMODIALYSIS SORBENT SYSTEM |
| Classification | System, Dialysate Delivery, Sorbent Regenerated |
| Applicant | RENAL SOLUTIONS, INC. 770 COMMONWEALTH DR. Warrendale, PA 15086 |
| Contact | David Vanella |
| Correspondent | David Vanella RENAL SOLUTIONS, INC. 770 COMMONWEALTH DR. Warrendale, PA 15086 |
| Product Code | FKT |
| CFR Regulation Number | 876.5600 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2012-12-13 |
| Decision Date | 2013-02-15 |
| Summary: | summary |