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

FRESENIUS F SERIES HEMOCONCENTRATORS F400,F500,F700,F800,F400TS,F500TS,F700S,F800TS

K Number: K974584 · Decision May 14, 1998
Classifications
1
FEI Numbers
81
Registration Numbers
81
Same Product Code
336
Applicant Total
38
Review Days
157

Basic Information

Device Name
FRESENIUS F SERIES HEMOCONCENTRATORS F400,F500,F700,F800,F400TS,F500TS,F700S,F800TS
K Number
K974584
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.5860
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
FRESENIUS USA, INC.
Date Received
December 8, 1997
Decision Date
May 14, 1998
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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K Number Device Name
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K973378 C.A.T.S CONTINUOUS AUTOTRANSFUSION SYSTEM MODEL 900500 1, AT1 AUTOTRANSFUSION SET MODEL 900 510 1, PSQ SET (DD) MODEL 61
K961465 2008H ON LINE CLEARANCE MONITOR
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K955762 PACKPD PERITONEAL DIALYSIS UREA KINETIC MODELING SOFTWARE PROGRAM
K941460 FRESENIUS BLOOD TEMPERATURE MONITOR
K955423 PACK H HEMODIALYSIS UREA KINETIC MODELING SOFTWARE PROGRAM
K944767 DIALYSIS MACHINE WITH DIALYSATE ULTRAFILTER
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Search all 38 clearances from FRESENIUS USA, INC. →