FDA 510(k) FDA class 1 Substantially Equivalent 🇪🇸 Spain

ADVIA Centaur EBV-VCA IgM

K Number: K233606 · Decision Aug 7, 2024
Classifications
1
FEI Numbers
15
Registration Numbers
15
Same Product Code
55
Applicant Total
23
Review Days
272

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
ADVIA Centaur EBV-VCA IgM
K Number
K233606
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
866.3235
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Biokit, S.A.
Date Received
November 9, 2023
Decision Date
August 7, 2024
Product Code
LSE
Advisory Committee
Microbiology
Review Advisory Committee
MI
Third Party
N

Classifications

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

Product Code Device Name
LSE Epstein-Barr Virus, Other

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (LSE), 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
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
K110619 ARCHITECT 25-OH VITAMIN D 100T, VITAMIN D 500T, VITAMIN D CALIBRATORS, VITAMIN D CONTROLS
Search all 23 clearances from Biokit, S.A. →