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

PHOSPHORUS REAGENT

K Number: K003912 · Decision Feb 21, 2001
Classifications
1
FEI Numbers
38
Registration Numbers
38
Same Product Code
104
Applicant Total
20
Review Days
64

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
PHOSPHORUS REAGENT
K Number
K003912
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.1580
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Jas Diagnostics, Inc.
Date Received
December 19, 2000
Decision Date
February 21, 2001
Product Code
CEO
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
CEO Phosphomolybdate (Colorimetric), Inorganic Phosphorus

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (CEO), ordered by most recent decision date.

View all

Other Clearances by Jas Diagnostics, Inc.

K Number Device Name
K130915 XL-200 CLINICAL CHEMISTRY ANALYZER, JAS GLUCOSE REAGENT, ISE REAGENT PACK
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
Search all 20 clearances from Jas Diagnostics, Inc. →