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

IMUBIND TPA ELISA, MODEL 860

K Number: K013492 · Decision Mar 13, 2002
Classifications
1
FEI Numbers
22
Registration Numbers
22
Same Product Code
188
Applicant Total
10
Review Days
142

Basic Information

Device Name
IMUBIND TPA ELISA, MODEL 860
K Number
K013492
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
864.7290
Medical Specialty
Hematology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
AMERICAN DIAGNOSTICA, INC.
Date Received
October 22, 2001
Decision Date
March 13, 2002
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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