The following data is part of a premarket notification filed by Cobe Laboratories, Inc. with the FDA for Dialysate Concentrate For Hemodialysis.
| Device ID | K810280 |
| 510k Number | K810280 |
| Device Name: | DIALYSATE CONCENTRATE FOR HEMODIALYSIS |
| Classification | Dialysate Concentrate For Hemodialysis (liquid Or Powder) |
| Applicant | COBE LABORATORIES, 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 | 1981-02-02 |
| Decision Date | 1981-02-19 |