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

SODIUM CITRATE

K Number: K761177 · Decision Jan 10, 1977
Classifications
1
FEI Numbers
6
Registration Numbers
6
Same Product Code
6
Applicant Total
37
Review Days
40

Basic Information

Device Name
SODIUM CITRATE
K Number
K761177
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1675
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
BIO/DATA CORP.
Date Received
December 1, 1976
Decision Date
January 10, 1977
Product Code
GJE
Advisory Committee
Clinical Chemistry
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
GJE Tray, Blood Collection

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