The following data is part of a premarket notification filed by Di-chem, Inc. with the FDA for Dialysate Additives-powder/liquid.
| Device ID | K823103 |
| 510k Number | K823103 |
| Device Name: | DIALYSATE ADDITIVES-POWDER/LIQUID |
| Classification | Dialysate Concentrate For Hemodialysis (liquid Or Powder) |
| Applicant | DI-CHEM, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | KPO |
| CFR Regulation Number | 876.5820 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1982-10-20 |
| Decision Date | 1982-11-17 |