FDA 510(k) FDA class 2 Substantially Equivalent 🇨🇦 Canada

VISULIZE FACTOR VIII ANTIGEN KIT, MODEL FVIII-AG

K Number: K052825 · Decision Jan 20, 2006
Classifications
1
FEI Numbers
21
Registration Numbers
21
Same Product Code
189
Applicant Total
5
Review Days
107

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Basic Information

Device Name
VISULIZE FACTOR VIII ANTIGEN KIT, MODEL FVIII-AG
K Number
K052825
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
864.7290
Medical Specialty
Hematology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Affinity Biologicals, Inc.
Date Received
October 5, 2005
Decision Date
January 20, 2006
Product Code
GGP
Advisory Committee
Hematology
Review Advisory Committee
HE
Third Party
N

Classifications

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

Product Code Device Name
GGP Test, Qualitative And Quantitative Factor Deficiency

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (GGP), ordered by most recent decision date.

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Other Clearances by Affinity Biologicals, Inc.

K Number Device Name
K150144 VisuCon-F Low Fibrinogen Control Plasma
K110432 VISUCON-F FROZEN COAG SCREEN N, VISUCON-F FROZEN COAG SCREEN ABN
K091284 VISUCAL-F FROZEN CALIBRATOR PLASMA AND VISUCON-F FROZEN NORMAL AND ABNORMAL CONTROL PLASMA
K051054 VISULIZE FACTOR IX ANTIGEN KIT