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

SYNERMEDIR CAL I AND SYNERMED IR CAL II

K Number: K940571 · Decision Apr 21, 1994
Classifications
1
FEI Numbers
101
Registration Numbers
101
Same Product Code
301
Applicant Total
45
Review Days
72

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Basic Information

Device Name
SYNERMEDIR CAL I AND SYNERMED IR CAL II
K Number
K940571
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1150
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Synermed, Inc.
Date Received
February 8, 1994
Decision Date
April 21, 1994
Product Code
JIX
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
JIX Calibrator, Multi-Analyte Mixture

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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. →