Multiple Artificial Kidney Systems (Maks) #Idm
K874084 is the FDA 510(k) clearance record for MULTIPLE ARTIFICIAL KIDNEY SYSTEMS (MAKS) #IDM, a class II device, cleared for National Medical Care, Medical Products Div., Inc. on under FDA product code FKQ (System, Dialysate Delivery, Central Multiple Patient). FDA records list 62 510(k) clearances for National Medical Care, Medical Products Div., Inc., from to . As of , FDA records show no recalls naming K874084.
Clearance record
- Decision date
- Received
- (203 days to decision)
- Product code
- FKQ System, Dialysate Delivery, Central Multiple Patient
- Regulation
- 21 CFR 876.5820
- Device class
- Class II
- Review panel
- Gastroenterology, Urology
- Applicant
- National Medical Care, Medical Products Div., Inc. Two Volvo Dr., Rockleigh NJ
- Third party review
- No
Clearances, product code FKQ
Trailing 12 monthsFDA records hold no clearances under product code FKQ in the trailing twelve months.
Show the numbers
| Month | Clearances |
|---|---|
| November 2025 | 0 |
| December 2025 | 0 |
| January 2026 | 0 |
| February 2026 | 0 |
| March 2026 | 0 |
| April 2026 | 0 |
| May 2026 | 0 |
| June 2026 | 0 |
| July 2026 | 0 |
| August 2026 | 0 |
| September 2026 | 0 |
| October 2026 | 0 |
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