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

THROMBOPLASTIN.R

K Number: K864274 · Decision Nov 13, 1986
Classifications
1
FEI Numbers
31
Registration Numbers
31
Same Product Code
126
Applicant Total
149
Review Days
15

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Basic Information

Device Name
THROMBOPLASTIN.R
K Number
K864274
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
864.7750
Medical Specialty
Hematology
Decision
Substantially Equivalent
Applicant
American Dade
Date Received
October 29, 1986
Decision Date
November 13, 1986
Product Code
GJS
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
GJS Test, Time, Prothrombin

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