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

QUANTIA LA(A)

K Number: K050487 · Decision Apr 26, 2005
Classifications
1
FEI Numbers
27
Registration Numbers
27
Same Product Code
42
Applicant Total
23
Review Days
60

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Basic Information

Device Name
QUANTIA LA(A)
K Number
K050487
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.5600
Medical Specialty
Immunology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Biokit, S.A.
Date Received
February 25, 2005
Decision Date
April 26, 2005
Product Code
DFC
Advisory Committee
Immunology
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
DFC Lipoprotein, Low-Density, Antigen, Antiserum, Control

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K152185 ARCHITECT SHBG
K132400 LP(A) CALIBRATORS, AND LP(A) CONTROLS
K123947 ARCHITECT IVANCOMYCIN
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