510(k) K874084

MULTIPLE ARTIFICIAL KIDNEY SYSTEMS (MAKS) #IDM by National Medical Care, Medical Products Div., Inc. — Product Code FKQ

K874084 is an FDA 510(k) premarket notification submitted by National Medical Care, Medical Products Div., Inc. for the device "MULTIPLE ARTIFICIAL KIDNEY SYSTEMS (MAKS) #IDM". The FDA issued a decision of Substantially Equivalent on April 27, 1988. The device falls under product code FKQ (System, Dialysate Delivery, Central Multiple Patient), a Class II device regulated under 21 CFR 876.5820. National Medical Care, Medical Products Div., Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
April 27, 1988
Date Received
October 7, 1987
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
System, Dialysate Delivery, Central Multiple Patient
Device Class
Class II
Regulation Number
876.5820
Review Panel
GU
Submission Type