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

ASSERACHROM VWF KIT

K Number: K860371 · Decision Apr 4, 1986
Classifications
1
FEI Numbers
22
Registration Numbers
22
Same Product Code
188
Applicant Total
79
Review Days
60

Basic Information

Device Name
ASSERACHROM VWF KIT
K Number
K860371
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
864.7290
Medical Specialty
Hematology
Decision
Substantially Equivalent
Applicant
AMERICAN BIOPRODUCTS CO.
Date Received
February 3, 1986
Decision Date
April 4, 1986
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

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