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

ALBUMIN TEST

K Number: K811662 · Decision Jun 25, 1981
Classifications
1
FEI Numbers
38
Registration Numbers
38
Same Product Code
119
Applicant Total
41
Review Days
10

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Basic Information

Device Name
ALBUMIN TEST
K Number
K811662
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1035
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
King Diagnostics, Inc.
Date Received
June 15, 1981
Decision Date
June 25, 1981
Product Code
CIX
Advisory Committee
Clinical Chemistry
Review Advisory Committee
CH
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
CIX Bromcresol Green Dye-Binding, Albumin

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K931773 HDL PRECIPITATING REAGENT (DEXTRAN SULFATE)
K931326 KING DIAGNOSTICS CK REAGENT
K923129 KING DIAGNOSTICS GLUCOSE (HK) REAGENT
K922969 KING DIAGNOSTICS UREA NITROGEN REAGENT
K922921 KING DIAGNOSTICS CHLORIDE REAGENT
K923927 KING DIAGNOSTICS MAGNESIUM REAGENT
K923091 KING DIAGNOSTICS GAMMA GT REAGENT
K923128 KING DIAGNOSTICS CHOLESTEROL REAGENT
Search all 41 clearances from King Diagnostics, Inc. →