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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
LTJ
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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
K
24
0403
Access BR Monitor
2
Cleared 510(K)
K
23
3946
IMMULITE® 2000 BR-MA
2
Cleared 510(K)
K
19
2524
Lumipulse G CA15-3
2
Cleared 510(K)
K
19
3489
ADVIA Centaur BR
2
Cleared 510(K)
K
19
2777
ADVIA Centaur CA 15-3 assay
2
Cleared 510(K)
K
18
1492
Elecsys CA 15-3 II
2
Cleared 510(K)
K
17
1605
Elecsys CA 15-3 II
2
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K
10
0344
DIMENSION VISTA LOCI CA 15-3 FLEX REAGENT CARTRIDGE, DIMENSION VISTA LOCI 7 CALIBRATOR, MODELS: K6456 AND KC605
2
Cleared 510(K)
K
07
2612
ACCESS IMMUNOASSAY SYSTEMS BR MONITOR, AND CALIBRATORS, MODEL(S) 387620,AND 387647
2
Cleared 510(K)
K
04
2732
ARCHITECT CA 15-3 ASSAY
2
Cleared 510(K)
Show All 28 Submissions
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
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Last synced on 27 June 2025 at 11:06 pm
IM
/
subpart-g—tumor-associated-antigen-immunological-test-systems
/
MOI
/
K181492
View Source
Elecsys CA 15-3 II
Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K181492
510(k) Type
Traditional
Applicant
Roche Diagnostics
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/22/2018
Days to Decision
16 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
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
K
24
0403
Access BR Monitor
K
23
3946
IMMULITE® 2000 BR-MA
K
19
2524
Lumipulse G CA15-3
K
19
3489
ADVIA Centaur BR
K
19
2777
ADVIA Centaur CA 15-3 assay
K
18
1492
Elecsys CA 15-3 II
K
17
1605
Elecsys CA 15-3 II
K
10
0344
DIMENSION VISTA LOCI CA 15-3 FLEX REAGENT CARTRIDGE, DIMENSION VISTA LOCI 7 CALIBRATOR, MODELS: K6456 AND KC605
K
07
2612
ACCESS IMMUNOASSAY SYSTEMS BR MONITOR, AND CALIBRATORS, MODEL(S) 387620,AND 387647
K
04
2732
ARCHITECT CA 15-3 ASSAY
Show All 28 Submissions
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
/
MOI
/
K181492
View Source
Elecsys CA 15-3 II
Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K181492
510(k) Type
Traditional
Applicant
Roche Diagnostics
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/22/2018
Days to Decision
16 days
Submission Type
Summary