The following data is part of a premarket notification filed by National Medical Care, Medical Products Div., Inc. with the FDA for Multiple Artificial Kidney Systems (maks) #idm.
| Device ID | K874084 |
| 510k Number | K874084 |
| Device Name: | MULTIPLE ARTIFICIAL KIDNEY SYSTEMS (MAKS) #IDM |
| Classification | System, Dialysate Delivery, Central Multiple Patient |
| Applicant | NATIONAL MEDICAL CARE, MEDICAL PRODUCTS DIV., INC. TWO VOLVO DR. Rockleigh, NJ 07647 |
| Contact | Del Donna |
| Correspondent | Del Donna NATIONAL MEDICAL CARE, MEDICAL PRODUCTS DIV., INC. TWO VOLVO DR. Rockleigh, NJ 07647 |
| Product Code | FKQ |
| CFR Regulation Number | 876.5820 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1987-10-07 |
| Decision Date | 1988-04-27 |