FDA 510(k) FDA class 1 Substantially Equivalent 🇨🇦 Canada

SYNERMED CHOLESTEROL REAGENT KIT

K Number: K903015 · Decision Oct 1, 1990
Classifications
1
FEI Numbers
82
Registration Numbers
82
Same Product Code
229
Applicant Total
45
Review Days
83

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Basic Information

Device Name
SYNERMED CHOLESTEROL REAGENT KIT
K Number
K903015
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.1175
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Synermed, Inc.
Date Received
July 10, 1990
Decision Date
October 1, 1990
Product Code
CHH
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
CHH Enzymatic Esterase--Oxidase, Cholesterol

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K Number Device Name
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K972716 SYNERMED TOTAL BILIRUBIN REAGENT KIT
K971491 SYNERMED IR 200 CHEMISTRY ANALYZER
K962479 SYNERMED ISE REAGENTS
K963939 SYNERMED DIRECT BILIRUBIN REAGENT KIT
K960793 SYNERMED ENZYMATIC CO2 REAGENT KIT
K953395 SYNERMED CALCIUM REAGENT KIT
K952179 SYNERMED ISE REAGENTS
K943924 CREATININE-PO REAGENT KIT
K941091 SYNERMED AMYLASE REAGENT KIT
Search all 45 clearances from Synermed, Inc. →