FDA 510(k) FDA unclassified Substantially Equivalent 🇺🇸 United States

P1R PLASMA TREATMENT SET FOR USE IN PLASMAPHERESIS WITH THE FRESENIUS AS104 CELL SEPARATOR

K Number: K961706 · Decision Jul 31, 1996
Classifications
1
FEI Numbers
20
Registration Numbers
20
Same Product Code
26
Applicant Total
38
Review Days
90

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Basic Information

Device Name
P1R PLASMA TREATMENT SET FOR USE IN PLASMAPHERESIS WITH THE FRESENIUS AS104 CELL SEPARATOR
K Number
K961706
Device Class
FDA unclassified
Clearance Type
Traditional
Medical Specialty
Unknown
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Fresenius USA, Inc.
Date Received
May 2, 1996
Decision Date
July 31, 1996
Product Code
LKN
Advisory Committee
Unknown
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
LKN Separator, Automated, Blood Cell And Plasma, Therapeutic

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Other Clearances by Fresenius USA, Inc.

K Number Device Name
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K970700 FRESENIUS POLYSULFONE HEMODIALYZERS, BOTH LOW AND HIGH FLUX
K974584 FRESENIUS F SERIES HEMOCONCENTRATORS F400,F500,F700,F800,F400TS,F500TS,F700S,F800TS
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
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
K930181 BIOPURE DIALYSATE CONCENTRATE MIX SYST/CONCENTRATE
Search all 38 clearances from Fresenius USA, Inc. →