510(k) K921456

FRESENIUS 3008/FDS-08 DIALYSATE DELIVERY SYSTEM by Fresenius USA, Inc. — Product Code FKP

K921456 is an FDA 510(k) premarket notification submitted by Fresenius USA, Inc. for the device "FRESENIUS 3008/FDS-08 DIALYSATE DELIVERY SYSTEM". The FDA issued a decision of Substantially Equivalent on April 20, 1994. The device falls under product code FKP (System, Dialysate Delivery, Single Patient), a Class II device regulated under 21 CFR 876.5820. Fresenius USA, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
April 20, 1994
Date Received
March 27, 1992
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

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