510(k) K060381

ALLIENT SORBET HEMODIALYSIS SYSTEM, MODEL 1100 by Renal Solutions, Inc. — Product Code FKT

K060381 is an FDA 510(k) premarket notification submitted by Renal Solutions, Inc. for the device "ALLIENT SORBET HEMODIALYSIS SYSTEM, MODEL 1100". The FDA issued a decision of Substantially Equivalent on May 24, 2006. The device falls under product code FKT (System, Dialysate Delivery, Sorbent Regenerated), a Class II device regulated under 21 CFR 876.5600. Renal Solutions, Inc. has at least 8 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
May 24, 2006
Date Received
February 14, 2006
Clearance Type
Special
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
System, Dialysate Delivery, Sorbent Regenerated
Device Class
Class II
Regulation Number
876.5600
Review Panel
GU
Submission Type