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

TRACE REAGENT LINE FOR THE COBAS MIRA

K Number: K973869 · Decision Jan 7, 1998
Classifications
1
FEI Numbers
44
Registration Numbers
44
Same Product Code
126
Applicant Total
22
Review Days
105

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Basic Information

Device Name
TRACE REAGENT LINE FOR THE COBAS MIRA
K Number
K973869
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.1030
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Trace America, Inc.
Date Received
September 24, 1997
Decision Date
January 7, 1998
Product Code
CKA
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
CKA Nadh Oxidation/Nad Reduction, Alt/Sgpt

Similar 510(k) Clearances

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Other Clearances by Trace America, Inc.

K Number Device Name
K003583 LITHIUM REGENT MODEL TR66056 / LITHIUM STANDARD TR66901
K980026 GLUCOSE (HK) - INCORPORATING DYNAMIC STABILIZATION TECHNOLOGY - (DST)
K980028 ALT (GPT) LIQUID STABLE 2 VIAL - INCORPORATING DYNAMIC STABILIZATION TECHNOLOGY - (DST)
K980030 AST )GOT) LIQUID STABLE 2 VIAL - INCORPORATING DYNAMIC STABILIZATION TECHNOLOGY - (DST)
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
K961984 PORPHOBILINOGEN (PBG)
Search all 22 clearances from Trace America, Inc. →