FDA 510(k) FDA class 2 Substantially Equivalent 🇨🇦 Canada

SYNERMED ISE REAGENTS

K Number: K962479 · Decision Mar 3, 1997
Classifications
1
FEI Numbers
84
Registration Numbers
84
Same Product Code
37
Applicant Total
45
Review Days
250

Basic Information

Device Name
SYNERMED ISE REAGENTS
K Number
K962479
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1170
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
SYNERMED, INC.
Date Received
June 26, 1996
Decision Date
March 3, 1997
Product Code
CGZ
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
CGZ Electrode, Ion-Specific, Chloride

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K Number Device Name
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K971491 SYNERMED IR 200 CHEMISTRY ANALYZER
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
K941400 SYNERMED ISE REAGENTS
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