510(k) K844750

FRESENIUS A2008 HEMODIALYSIS MACHINE EXPANSION MOD by Seratronics, Inc. — Product Code FKQ

K844750 is an FDA 510(k) premarket notification submitted by Seratronics, Inc. for the device "FRESENIUS A2008 HEMODIALYSIS MACHINE EXPANSION MOD". The FDA issued a decision of Substantially Equivalent on February 15, 1985. The device falls under product code FKQ (System, Dialysate Delivery, Central Multiple Patient), a Class II device regulated under 21 CFR 876.5820. Seratronics, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
February 15, 1985
Date Received
December 6, 1984
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