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

VITALAB MAGNESIUM REAGENT

K Number: K040508 · Decision Mar 8, 2004
Classifications
1
FEI Numbers
44
Registration Numbers
44
Same Product Code
89
Applicant Total
36
Review Days
10

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Basic Information

Device Name
VITALAB MAGNESIUM REAGENT
K Number
K040508
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.1495
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Clinical Data, Inc.
Date Received
February 27, 2004
Decision Date
March 8, 2004
Product Code
JGJ
Advisory Committee
Clinical Chemistry
Review Advisory Committee
CH
Third Party
Y

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
JGJ Photometric Method, Magnesium

Similar 510(k) Clearances

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

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Other Clearances by Clinical Data, Inc.

K Number Device Name
K071706 ENVOY 500 HDL; CHOLESTEROL REAGENT KIT (MODEL# 55301), CALIBRATOR KIT (MODEL# 55118)
K052591 NANOPIA WIDE RANGE C-REACTIVE PROTEIN (CRP) REAGENT KIT
K033983 VITALAB IRON REAGENT
K040631 VITALAB DIRECT BILIRUBIN REAGENT
K040534 VITALAB AMYLASE REAGENT
K034000 VITALAB TRIGLYCERIDES REAGENT AND VITALAB CALIBRATOR
K040467 VITALAB URIC ACID REAGENT
K031042 ATAC HEMOGLOBIN A1C REAGENT KIT
K031044 ATAC PAK URIC ACID REAGENT AND ATAC CALIBRATOR
K863904 DISPOSABLE ECG MONITORING ELECTRODE
Search all 36 clearances from Clinical Data, Inc. →