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

TRACE MAGNESIUM - ARSENAZO REAGENT

K Number: K920603 · Decision Mar 11, 1992
Classifications
1
FEI Numbers
44
Registration Numbers
44
Same Product Code
89
Applicant Total
22
Review Days
39

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Basic Information

Device Name
TRACE MAGNESIUM - ARSENAZO REAGENT
K Number
K920603
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.1495
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Trace America, Inc.
Date Received
February 1, 1992
Decision Date
March 11, 1992
Product Code
JGJ
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
JGJ Photometric Method, Magnesium

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K980028 ALT (GPT) LIQUID STABLE 2 VIAL - INCORPORATING DYNAMIC STABILIZATION TECHNOLOGY - (DST)
K980030 AST )GOT) LIQUID STABLE 2 VIAL - INCORPORATING DYNAMIC STABILIZATION TECHNOLOGY - (DST)
K973869 TRACE REAGENT LINE FOR THE COBAS MIRA
K974620 AMMONIA-INCORPORATING DYNAMIC STABILIZATION TECHNOLOGY (DST)
K972297 AMYLASE-INCORPORATING DYNAMIC STABILIZATION TECHNOLOGY - (DST)
K971477 UREA (UREA NITROGEN) - INCORPORATING DYNAMIC STABILIZATION TECHNOLOGY (DST)
K971485 URIC ACID - INCORPORATING DYNAMIC STABILIZATION TECHNOLOGY - (DST)
K962723 TRACE HDL CHOLESTEROL - AUTOMATED (HOMOGEN
Search all 22 clearances from Trace America, Inc. →