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

QUANTIA BETA-2 MICROGLOBULIN, MODEL: 302822307

K Number: K072078 · Decision Dec 19, 2007
Classifications
1
FEI Numbers
34
Registration Numbers
34
Same Product Code
52
Applicant Total
23
Review Days
142

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
QUANTIA BETA-2 MICROGLOBULIN, MODEL: 302822307
K Number
K072078
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.5630
Medical Specialty
Immunology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Biokit, S.A.
Date Received
July 30, 2007
Decision Date
December 19, 2007
Product Code
JZG
Advisory Committee
Immunology
Review Advisory Committee
IM
Third Party
N

Classifications

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

Product Code Device Name
JZG System, Test, Beta-2-Microglobulin Immunological

Similar 510(k) Clearances

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

View all

Other Clearances by Biokit, S.A.

K Number Device Name
K243575 ARCHITECT HSV-2 IgG, ARCHITECT HSV-2 IgG Calibrator, ARCHITECT HSV-2 IgG Controls
K233606 ADVIA Centaur EBV-VCA IgM
K233605 ADVIA Centaur EBV-EBNA IgG
K213987 ARCHITECT HSV-1 IgG, ARCHITECT HSV-1 IgG Calibrator, ARCHITECT HSV-1 IgG Controls
K214068 Quantia IgE
K181334 ADVIA Centaur Herpes-2 IgG
K181333 ADVIA Centaur Herpes-1 IgG
K152185 ARCHITECT SHBG
K132400 LP(A) CALIBRATORS, AND LP(A) CONTROLS
K123947 ARCHITECT IVANCOMYCIN
Search all 23 clearances from Biokit, S.A. →