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Subpart C—Clinical Laboratory Instruments
CFR Sub-Part
Subpart C—Microbiology Devices
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Subpart D—Clinical Toxicology Test Systems
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Subpart D—Serological Reagents
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Subpart E—Immunology Laboratory Equipment and Reagents
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Subpart G—Tumor Associated Antigen immunological Test Systems
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DHX
System, Test, Carcinoembryonic Antigen
2
Product Code
LOJ
Kit, Test,Alpha-Fetoprotein For Testicular Cancer
2
Product Code
K
22
0176
Elecsys AFP
2
Cleared 510(K)
K
21
3626
VITROS AFP
2
Cleared 510(K)
K
09
0236
DIMENSION VISTA AFP FLEX REAGENT CARTRIDGE, MODEL 6454
2
Cleared 510(K)
K
08
1709
OLYMPUS AFP - ALPHA-FETOPROTEIN
2
Cleared 510(K)
K
08
0017
VIDAS AFP ASSAY
2
Cleared 510(K)
K
07
1597
DIMENSION VISTA (R) AFP FLEX(R) REAGENT CARTRIDGE, MODEL K6454, DIMENSION VISTA (R) LOCI 5 CALIBRATOR, MODEL KC600
2
Cleared 510(K)
K
02
3894
ST AIA-PACK AFP ENZYME IMMUNOASSAY
2
Cleared 510(K)
K
02
0807
AFP ASSAY FOR THE ADVIA INTEGRATED MODULAR SYSTEM
2
Cleared 510(K)
K
02
0806
ACS:180 & ADVIA CENTAUR AFP IMMUNOASSAY
2
Cleared 510(K)
K
99
0138
DSL ACTIVE AFP ELISA, MODEL DSL-10-8400
2
Cleared 510(K)
Show All 17 Submissions
LTJ
Prostate-Specific Antigen (Psa) For Management Of Prostate Cancers
2
Product Code
LTK
Test, Epithelial Ovarian Tumor-Associated Antigen (Ca125)
2
Product Code
MMW
System, Test, Tumor Marker, Monitoring, Bladder
2
Product Code
MOI
System, Test, Immunological, Antigen, Tumor
2
Product Code
MSW
System, Test, Thyroglobulin
2
Product Code
MUT
Kit, Test For Nuclear Matrix (Numa) Protein (For Monitoring And Management Of Colorectal Cancer)
2
Product Code
NCW
System, Test, Her-2/Neu, Monitoring
2
Product Code
NIG
System, Test, Carbohydrate Antigen (Ca19-9), For Monitoring And Management Of Pancreatic Cancer
2
Product Code
NSF
Test, Alpha Fetoprotein L3 Subfraction (Afp-L3%), For Hepatocellular Carcinoma Risk Assessment
2
Product Code
NTY
System, Test, Fibrin/Fibrinogen Degradation Products For Monitoring Of Colorectal Cancer
2
Product Code
NVA
Cancer Monitoring Test System, Soluble Mesothelin-Related Peptides, Mesothelioma
2
Product Code
OAU
Des-Gamma-Carboxy-Prothrombin (Dcp), Risk Assessment, Hepatocellular Carcinoma
2
Product Code
OIU
Test, Epithelial Ovarian Tumor Associated Antigen (He4)
2
Product Code
OVK
Cytokeratin Fragments 21-1 Eia Kit
2
Product Code
ONX
Ovarian Adnexal Mass Assessment Score Test System
2
Product Code
QTE
Thymidine Kinase Activity
2
Product Code
QXS
Chromogranin A
2
Product Code
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Last synced on 11 July 2025 at 11:06 pm
IM
/
subpart-g—tumor-associated-antigen-immunological-test-systems
/
LOJ
/
K090236
View Source
DIMENSION VISTA AFP FLEX REAGENT CARTRIDGE, MODEL 6454
Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K090236
510(k) Type
Traditional
Applicant
SIEMENS HEALTHCARE DIAGNOSTICS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/27/2009
Days to Decision
84 days
Submission Type
Summary
FDA Browser
by
Innolitics
Anesthesiology
Cardiovascular
Chemistry
Dental
Ear, Nose, Throat
Gastroenterology and Urology
General Hospital
Hematology
Immunology
Miscellaneous
Subpart C—Clinical Laboratory Instruments
Subpart C—Microbiology Devices
Subpart D—Clinical Toxicology Test Systems
Subpart D—Serological Reagents
Subpart E—Immunology Laboratory Equipment and Reagents
Subpart E—Specimen Preparation Reagents
Subpart F—Automated and Semi-Automated Hematology Devices
Subpart F—Immunological Test Systems
Subpart G—Tumor Associated Antigen immunological Test Systems
DHX
System, Test, Carcinoembryonic Antigen
LOJ
Kit, Test,Alpha-Fetoprotein For Testicular Cancer
K
22
0176
Elecsys AFP
K
21
3626
VITROS AFP
K
09
0236
DIMENSION VISTA AFP FLEX REAGENT CARTRIDGE, MODEL 6454
K
08
1709
OLYMPUS AFP - ALPHA-FETOPROTEIN
K
08
0017
VIDAS AFP ASSAY
K
07
1597
DIMENSION VISTA (R) AFP FLEX(R) REAGENT CARTRIDGE, MODEL K6454, DIMENSION VISTA (R) LOCI 5 CALIBRATOR, MODEL KC600
K
02
3894
ST AIA-PACK AFP ENZYME IMMUNOASSAY
K
02
0807
AFP ASSAY FOR THE ADVIA INTEGRATED MODULAR SYSTEM
K
02
0806
ACS:180 & ADVIA CENTAUR AFP IMMUNOASSAY
K
99
0138
DSL ACTIVE AFP ELISA, MODEL DSL-10-8400
Show All 17 Submissions
LTJ
Prostate-Specific Antigen (Psa) For Management Of Prostate Cancers
LTK
Test, Epithelial Ovarian Tumor-Associated Antigen (Ca125)
MMW
System, Test, Tumor Marker, Monitoring, Bladder
MOI
System, Test, Immunological, Antigen, Tumor
MSW
System, Test, Thyroglobulin
MUT
Kit, Test For Nuclear Matrix (Numa) Protein (For Monitoring And Management Of Colorectal Cancer)
NCW
System, Test, Her-2/Neu, Monitoring
NIG
System, Test, Carbohydrate Antigen (Ca19-9), For Monitoring And Management Of Pancreatic Cancer
NSF
Test, Alpha Fetoprotein L3 Subfraction (Afp-L3%), For Hepatocellular Carcinoma Risk Assessment
NTY
System, Test, Fibrin/Fibrinogen Degradation Products For Monitoring Of Colorectal Cancer
NVA
Cancer Monitoring Test System, Soluble Mesothelin-Related Peptides, Mesothelioma
OAU
Des-Gamma-Carboxy-Prothrombin (Dcp), Risk Assessment, Hepatocellular Carcinoma
OIU
Test, Epithelial Ovarian Tumor Associated Antigen (He4)
OVK
Cytokeratin Fragments 21-1 Eia Kit
ONX
Ovarian Adnexal Mass Assessment Score Test System
QTE
Thymidine Kinase Activity
QXS
Chromogranin A
Microbiology
Neurology
Obstetrical and Gynecological
Ophthalmic
Orthopedic
Pathology
Physical Medicine
Radiology
General and Plastic Surgery
Toxicology
Medical Genetics
Unknown
IM
/
subpart-g—tumor-associated-antigen-immunological-test-systems
/
LOJ
/
K090236
View Source
DIMENSION VISTA AFP FLEX REAGENT CARTRIDGE, MODEL 6454
Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K090236
510(k) Type
Traditional
Applicant
SIEMENS HEALTHCARE DIAGNOSTICS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/27/2009
Days to Decision
84 days
Submission Type
Summary