The following data is part of a premarket notification filed by Renal Systems, Inc. with the FDA for Hpr Home Patient Renatron.
| Device ID | K833181 |
| 510k Number | K833181 |
| Device Name: | HPR HOME PATIENT RENATRON |
| Classification | Dialyzer Reprocessing System |
| Applicant | RENAL SYSTEMS, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | LIF |
| CFR Regulation Number | 876.5820 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1983-09-19 |
| Decision Date | 1983-10-27 |