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

XL-200 CLINICAL CHEMISTRY ANALYZER, JAS GLUCOSE REAGENT, ISE REAGENT PACK

K Number: K130915 · Decision May 15, 2014
Classifications
1
FEI Numbers
174
Registration Numbers
174
Same Product Code
207
Applicant Total
20
Review Days
408

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Basic Information

Device Name
XL-200 CLINICAL CHEMISTRY ANALYZER, JAS GLUCOSE REAGENT, ISE REAGENT PACK
K Number
K130915
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.2160
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Jas Diagnostics, Inc.
Date Received
April 2, 2013
Decision Date
May 15, 2014
Product Code
JJE
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
JJE Analyzer, Chemistry (Photometric, Discrete), For Clinical Use

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Other Clearances by Jas Diagnostics, Inc.

K Number Device Name
K080623 CHOLESTEROL OXIDASE JASE, AND GLYCEROL INASE TRIGLYCERIDES, MODEL NA
K080618 DIRECT HBA1C, FRUCTOSAMINE, GLUCOSE OXIDASE LIQUID
K022519 LDL CHOLESTEROL (AUTOMATED)
K021671 JAS HDL CHOLESTEROL (AUTOMATED) REAGENT
K020454 CHEMISTRY CALIBRATOR
K020282 JAS AMYLASE LIQUID REAGENT
K013912 CREATINE KINASE (CK-NAC)
K013698 AST (SGOT)
K012332 JAS CARBON DIOXIDE LIQUID REAGENT
K012038 JAS URIC ACID LIQUID REAGENT
Search all 20 clearances from Jas Diagnostics, Inc. →