FDA 510(k) FDA class 2 Substantially Equivalent 🇪🇸 Spain

ARCHITECT 25-OH VITAMIN D 100T, VITAMIN D 500T, VITAMIN D CALIBRATORS, VITAMIN D CONTROLS

K Number: K110619 · Decision Nov 23, 2011
Classifications
1
FEI Numbers
51
Registration Numbers
51
Same Product Code
45
Applicant Total
23
Review Days
265

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Basic Information

Device Name
ARCHITECT 25-OH VITAMIN D 100T, VITAMIN D 500T, VITAMIN D CALIBRATORS, VITAMIN D CONTROLS
K Number
K110619
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1825
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Biokit, S.A.
Date Received
March 3, 2011
Decision Date
November 23, 2011
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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