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

SYNERMED ALKALINE PHOSPHATASE REAGENT KIT

K Number: K904030 · Decision Sep 27, 1990
Classifications
1
FEI Numbers
37
Registration Numbers
37
Same Product Code
123
Applicant Total
45
Review Days
27

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Basic Information

Device Name
SYNERMED ALKALINE PHOSPHATASE REAGENT KIT
K Number
K904030
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1050
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Synermed, Inc.
Date Received
August 31, 1990
Decision Date
September 27, 1990
Product Code
CJE
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
CJE Nitrophenylphosphate, Alkaline Phosphatase Or Isoenzymes

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Other Clearances by Synermed, Inc.

K Number Device Name
K973109 SYNERMED NEAR-INFRARED DIRECT BILIRUBIN REAGENT KIT
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. →