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

SIGMA DIANOSTICS AUTO D-DIMER CONTROL LEVEL 2, MODEL A5217

K Number: K003329 · Decision Mar 1, 2001
Classifications
1
FEI Numbers
21
Registration Numbers
21
Same Product Code
39
Applicant Total
164
Review Days
128

Basic Information

Device Name
SIGMA DIANOSTICS AUTO D-DIMER CONTROL LEVEL 2, MODEL A5217
K Number
K003329
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
864.5425
Medical Specialty
Hematology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
SIGMA DIAGNOSTICS, INC.
Date Received
October 24, 2000
Decision Date
March 1, 2001
Product Code
GGC
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
GGC Control, Plasma, Abnormal

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