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

SODIUM REAGENT SET

K Number: K914039 · Decision Oct 31, 1991
Classifications
1
FEI Numbers
4
Registration Numbers
4
Same Product Code
3
Applicant Total
41
Review Days
51

Basic Information

Device Name
SODIUM REAGENT SET
K Number
K914039
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1665
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
STERLING DIAGNOSTICS, INC.
Date Received
September 10, 1991
Decision Date
October 31, 1991
Product Code
CEI
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
CEI Uranyl Acetate/Zinc Acetate, Sodium

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K Number Device Name
K921412 MICROPROTEIN REAGENT SET
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K914040 PHOSPHOLIPID REAGENT SET
K862255 LACTATE DEHYDROGENASE (LDH) REAGENT SET (UV RATE)
K861962 VANILMANDELIC ACID (VMA) REAGENT SET
K862256 ALKALINE PHOSPHATASE (PNPP RATE) REAGENT SET
K862210 UREA NITROGEN (GLDH) REAGENT SET (UV)
K862209 ALT (SGPT) REAGENT SET (UV RATE)
K861855 HYDROXYBUTYRATE DEHYDROGENASE (HBD) REAGENT SET
K861713 SERUM POTASSIUM REAGENT SET
Search all 41 clearances from STERLING DIAGNOSTICS, INC. →