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

COAGULATION FACTOR V DEFICIENT SUBSTR

K Number: K841364 · Decision Apr 25, 1984
Classifications
1
FEI Numbers
21
Registration Numbers
21
Same Product Code
189
Applicant Total
149
Review Days
23

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Basic Information

Device Name
COAGULATION FACTOR V DEFICIENT SUBSTR
K Number
K841364
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
864.7290
Medical Specialty
Hematology
Decision
Substantially Equivalent
Applicant
American Dade
Date Received
April 2, 1984
Decision Date
April 25, 1984
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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