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Innolitics
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Subpart C—Clinical Laboratory Instruments
CFR Sub-Part
Subpart C—Microbiology Devices
CFR Sub-Part
Subpart D—Clinical Toxicology Test Systems
CFR Sub-Part
Subpart D—Serological Reagents
CFR Sub-Part
Subpart E—Immunology Laboratory Equipment and Reagents
CFR Sub-Part
Subpart E—Specimen Preparation Reagents
CFR Sub-Part
Subpart F—Automated and Semi-Automated Hematology Devices
CFR Sub-Part
LIZ
Assay, T Lymphocyte Surface Marker
2
Product Code
LJD
Assay, B Lymphocyte Marker
2
Product Code
K
85
1639
ANTI-LEU-12 B CELL REAGENT
2
Cleared 510(K)
NID
Assay, Proliferation, In Vitro, T Lymphocyte
2
Product Code
PDX
Flow Cytometry Calibrator
2
Product Code
Subpart F—Immunological Test Systems
CFR Sub-Part
Subpart G—Tumor Associated Antigen immunological Test Systems
CFR Sub-Part
Microbiology
Review Panel
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Unknown
Review Panel
Last synced on 13 June 2025 at 11:06 pm
IM
/
subpart-f—automated-and-semi-automated-hematology-devices
/
LJD
/
K851639
View Source
ANTI-LEU-12 B CELL REAGENT
Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K851639
510(k) Type
Traditional
Applicant
BD BECTON DICKINSON VACUTAINER SYSTEMS PREANALYTIC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/2/1986
Days to Decision
439 days
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
LIZ
Assay, T Lymphocyte Surface Marker
LJD
Assay, B Lymphocyte Marker
K
85
1639
ANTI-LEU-12 B CELL REAGENT
NID
Assay, Proliferation, In Vitro, T Lymphocyte
PDX
Flow Cytometry Calibrator
Subpart F—Immunological Test Systems
Subpart G—Tumor Associated Antigen immunological Test Systems
Microbiology
Neurology
Obstetrical and Gynecological
Ophthalmic
Orthopedic
Pathology
Physical Medicine
Radiology
General and Plastic Surgery
Toxicology
Medical Genetics
Unknown
IM
/
subpart-f—automated-and-semi-automated-hematology-devices
/
LJD
/
K851639
View Source
ANTI-LEU-12 B CELL REAGENT
Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K851639
510(k) Type
Traditional
Applicant
BD BECTON DICKINSON VACUTAINER SYSTEMS PREANALYTIC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/2/1986
Days to Decision
439 days