FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

ULTRX(TM) 850 ARTIFICIAL KIDNEY

K Number: K884353 · Decision Dec 8, 1988
Classifications
1
FEI Numbers
89
Registration Numbers
89
Same Product Code
343
Applicant Total
11
Review Days
52

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Basic Information

Device Name
ULTRX(TM) 850 ARTIFICIAL KIDNEY
K Number
K884353
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.5860
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Applicant
Cd Medical, Inc.
Date Received
October 17, 1988
Decision Date
December 8, 1988
Product Code
KDI
Advisory Committee
Gastroenterology, Urology
Review Advisory Committee
GU
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
KDI Dialyzer, High Permeability With Or Without Sealed Dialysate System

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Other Clearances by Cd Medical, Inc.

K Number Device Name
K925654 CD HOME DIALYSERVICE HEMODIALYSIS TRAY
K910215 DRAKE WILLOCK SYSTEM 1000 DIALYSATE DELIVERY SYST
K901520 WURTZ CHOLEY CLIP (TM)
K894106 DRAKE WILLOCK REVERSE OSMOSIS WATER TREATMENT SYST
K880459 480 HIGH-FLOW ULTRAFILTRATION CONTROL DIALYSATE
K873279 8810 PUMP-PUMP SINGLE NEEDLE DEVICE
K864784 SERAFLO(TM) BLOODLINES FOR HEMODIALYSIS
K862304 DRAKE WILLOCK CENTRAL DIALYSATE DELIVERY SYSTEM
K853513 DRAKE WILLOCK 480 UF CONTROL IDALYSATE DELIVERY SY
K844185 MODIFIED C-DAK
Search all 11 clearances from Cd Medical, Inc. →