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

KING SODIUM/POTASSIUM STANDARD MODIFIED

K Number: K931834 · Decision Aug 25, 1993
Classifications
1
FEI Numbers
72
Registration Numbers
72
Same Product Code
129
Applicant Total
41
Review Days
152

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Basic Information

Device Name
KING SODIUM/POTASSIUM STANDARD MODIFIED
K Number
K931834
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1150
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
King Diagnostics, Inc.
Date Received
March 26, 1993
Decision Date
August 25, 1993
Product Code
JIS
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
JIS Calibrator, Primary

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Other Clearances by King Diagnostics, Inc.

K Number Device Name
K933329 KING DIAGNOSTICS IRON AND TOTAL IRON BINDING CAPACITY REAGENT
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
K922964 KING DIAGNOSTIC TRIGLYCERIDES REAGENT
Search all 41 clearances from King Diagnostics, Inc. →