FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

AMICON VITAFIBER FLO-PATH BIORECT/VLS CELL CULT SY

K Number: K892645 · Decision Jun 13, 1989
Classifications
1
FEI Numbers
23
Registration Numbers
23
Same Product Code
3
Applicant Total
20
Review Days
62

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Basic Information

Device Name
AMICON VITAFIBER FLO-PATH BIORECT/VLS CELL CULT SY
K Number
K892645
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
864.2240
Medical Specialty
Hematology
Decision
Substantially Equivalent
Applicant
Amicon, Inc.
Date Received
April 12, 1989
Decision Date
June 13, 1989
Product Code
KJF
Advisory Committee
Hematology
Review Advisory Committee
PA
Third Party
N

Classifications

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

Product Code Device Name
KJF System, Suspension, Cell Culture

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K Number Device Name
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K901286 AMICON HEMOCONCENTRATOR SET
K900280 CENTRIPREP 100
K895405 AMICON MINIFILTER PLUS HEMOFILTER
K893733 CENTRICON CONCENTRATOR
K875121 AMICON EQUALINE FLUID BALANCE SYSTEM
K870690 CENTRIPREP CONCENTRATOR
K863823 AMICON DIAFILTER HEMOFILTER
K853510 MINIFILTER HEMOFILTER
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