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

DATA-FI DIMERTEST LATEX ASSAY

K Number: K872195 · Decision Aug 6, 1987
Classifications
1
FEI Numbers
31
Registration Numbers
31
Same Product Code
56
Applicant Total
149
Review Days
59

Basic Information

Device Name
DATA-FI DIMERTEST LATEX ASSAY
K Number
K872195
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
864.7320
Medical Specialty
Hematology
Decision
Substantially Equivalent
Applicant
AMERICAN DADE
Date Received
June 8, 1987
Decision Date
August 6, 1987
Product Code
DAP
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
DAP Fibrinogen And Fibrin Split Products, Antigen, Antiserum, Control

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