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

ADVIA 120 HEMATOLOGY SYSTEM, CEREBROSPINAL FLUID METHOD

K Number: K022331 · Decision Sep 11, 2002
Classifications
1
FEI Numbers
21
Registration Numbers
21
Same Product Code
129
Applicant Total
32
Review Days
55

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Basic Information

Device Name
ADVIA 120 HEMATOLOGY SYSTEM, CEREBROSPINAL FLUID METHOD
K Number
K022331
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
864.5200
Medical Specialty
Hematology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Bayer Diagnostics Corp.
Date Received
July 18, 2002
Decision Date
September 11, 2002
Product Code
GKL
Advisory Committee
Hematology
Review Advisory Committee
HE
Third Party
N

Classifications

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

Product Code Device Name
GKL Counter, Cell, Automated (Particle Counter)

Similar 510(k) Clearances

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Other Clearances by Bayer Diagnostics Corp.

K Number Device Name
K033379 BAYER SPECIAL CHEMISTRY CONTROLS
K033380 BAYER SPECIAL CHEMISTRY CALIBRATORS
K033007 BAYER ADVIA DIGOXIN ASSAY FOR THE INTEGRATED MODULE SYSTEM
K031857 ADVIA CHEMISTRY ALPHA-1 ANTITRYPSIN ASSAY
K022096 URIC ACID ASSAY FOR THE ADVIA INTEGRATED MODULAR SYSTEM
K030452 BAYER LIGAND PLUS 1, 2, 3 CONTROLS
K023840 ACID PHOSPHATASE ASSAY FOR THE ADVIA 1650
K023841 AMMONIA ASSAY FOR THE ADVIA 1650
K022177 PROSTATE SPECIFIC ANTIGEN (PSA) ASSAY FOR THE ADVIA INTEGRATED MODULAR SYSTEM
K022329 CA 125 II ASSAY FOR THE BAYER ADVIA INTEGRATED MODULE SYSTEM
Search all 32 clearances from Bayer Diagnostics Corp. →