FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

25-OH VITAMIN D ELISA

K Number: K123660 · Decision Jul 17, 2013
Classifications
1
FEI Numbers
51
Registration Numbers
51
Same Product Code
45
Applicant Total
12
Review Days
231

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Basic Information

Device Name
25-OH VITAMIN D ELISA
K Number
K123660
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1825
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Euroimmun US
Date Received
November 28, 2012
Decision Date
July 17, 2013
Product Code
MRG
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
MRG System, Test, Vitamin D

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