FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

SIGMA PROCEDURE & REAGENT SYSTEM #335-UV

K Number: K800301 · Decision Mar 5, 1980
Classifications
1
FEI Numbers
39
Registration Numbers
39
Same Product Code
150
Applicant Total
231
Review Days
23

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Basic Information

Device Name
SIGMA PROCEDURE & REAGENT SYSTEM #335-UV
K Number
K800301
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.1705
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Sigma Chemical Co.
Date Received
February 11, 1980
Decision Date
March 5, 1980
Product Code
CDT
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
CDT Lipase Hydrolysis/Glycerol Kinase Enzyme, Triglycerides

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Other Clearances by Sigma Chemical Co.

K Number Device Name
K933694 SIGMA GLUCOSE REAGENT
K933678 SIGMA CALCIUM REAGENT
K933696 SIGMA ELECTROLYTE REFERENCE REAGENT
K933679 SIGMA BUN REAGENT
K933691 SIGMA CO2 ALKALINE BUFFER REAGENT
K933703 SIGMA WASH CONCENTRATE SOLUTION
K933692 SIGMA CO2 ACID REAGENT
K933695 SIGMA ELECTROLYTE BUFFER
K933697 SIGMA CRE REAGENT
K933693 SIGMA CX-3 CALIBRATION STANDARD LEVEL 2
Search all 231 clearances from Sigma Chemical Co. →