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Review Panel
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Review Panel
Miscellaneous
Miscellaneous
Subpart B—Biological Stains
CFR Sub-Part
Subpart B—Diagnostic Devices
CFR Sub-Part
Subpart C—Cell And Tissue Culture Products
CFR Sub-Part
Subpart C—Clinical Laboratory Instruments
CFR Sub-Part
Subpart E—Specimen Preparation Reagents
CFR Sub-Part
Subpart F—Automated and Semi-Automated Hematology Devices
CFR Sub-Part
Subpart F—General Hospital and Personal Use Therapeutic Devices
CFR Sub-Part
Subpart F—Immunological Test Systems
CFR Sub-Part
Subpart G—Manual Hematology Devices
CFR Sub-Part
Subpart G—Tumor Associated Antigen immunological Test Systems
CFR Sub-Part
Subpart H—Hematology Kits and Packages
CFR Sub-Part
Subpart I—Hematology Reagents
CFR Sub-Part
GIR
Reagent, Russel Viper Venom
1
Product Code
GJN
Fluid, Diluting, Red-Cell
1
Product Code
GJP
Control, Platelet
2
Product Code
GJR
Control, Red-Cell
2
Product Code
GFS
Standards And Controls, Hemoglobin, Normal And Abnormal
2
Product Code
GGJ
Fluid, Diluting, White-Cell
1
Product Code
GGK
Products, Red-Cell Lysing Products
1
Product Code
GGL
Control, White-Cell
2
Product Code
GGM
Control, Hemoglobin
2
Product Code
GIF
Diluent, Blood Cell
1
Product Code
GLK
Control, Hematocrit
2
Product Code
GLQ
Mixture, Control, White-Cell And Red-Cell Indices
2
Product Code
JCF
Lymphocyte Separation Medium
1
Product Code
K
91
1731
LEUCOPREP(R) BRAND CELL SEPARAT TUBE W/SODIUM CITR
1
Cleared 510(K)
K
90
2445
LYMPHO SEP(TM)
1
Cleared 510(K)
K
89
1407
LEUCOPREP CELL SEPARATION TUBE
1
Cleared 510(K)
K
87
4328
L-PHENYLALANINE METHYL ESTER HYDROCHLORIDE PME REA
1
Cleared 510(K)
K
87
3185
DYNABEADS HLA CELL PREP II ISOLATION PRODUCT
1
Cleared 510(K)
K
87
2775
LEUCOPREP BRAND TUBE
1
Cleared 510(K)
K
86
0354
SEPRACELL LYMPHOCYTE SEPARATION MEDIUM
1
Cleared 510(K)
K
85
4093
LEUCO PREP
1
Cleared 510(K)
K
84
2818
CST
1
Cleared 510(K)
K
84
2146
HISTOPAQUE-1077
1
Cleared 510(K)
Show All 12 Submissions
JCG
Fluid, Diluting, Manual Cell
1
Product Code
JCN
Control, Cell Counter, Normal And Abnormal
2
Product Code
JCO
Bothrops Atrox Reagent
2
Product Code
JPK
Mixture, Hematology Quality Control
2
Product Code
KRX
Calibrator For Cell Indices
2
Product Code
KRY
Calibrator For Platelet Counting
2
Product Code
KRZ
Calibrator For Hemoglobin And Hematocrit Measurement
2
Product Code
KSA
Calibrator For Red-Cell And White-Cell Counting
2
Product Code
MZG
Test, Residual, Wbc In Leukoreduced Blood
2
Product Code
NRF
Material, Quality Control, Semen Analysis
2
Product Code
NRS
Control Material, Blood Circulating Epithelial Cancer Cell
2
Product Code
Subpart J—Products Used In Establishments That Manufacture Blood and Blood Products
CFR Sub-Part
Subpart K—Products Used In Establishments That Manufacture Human Cells, Tissues, and Cellular and Tissue-Based Products (HCT/Ps)
CFR Sub-Part
Immunology
Review Panel
Microbiology
Review Panel
Neurology
Review Panel
Obstetrical and Gynecological
Review Panel
Ophthalmic
Review Panel
Orthopedic
Review Panel
Pathology
Review Panel
Physical Medicine
Review Panel
Radiology
Review Panel
General and Plastic Surgery
Review Panel
Toxicology
Review Panel
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Review Panel
Unknown
Review Panel
Last synced on 16 May 2025 at 11:05 pm
HE
/
subpart-i—hematology-reagents
/
JCF
/
K902445
View Source
LYMPHO SEP(TM)
Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K902445
510(k) Type
Traditional
Applicant
ICN BIOMEDICALS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/22/1990
Days to Decision
82 days
FDA Browser
by
Innolitics
Anesthesiology
Cardiovascular
Chemistry
Dental
Ear, Nose, Throat
Gastroenterology and Urology
General Hospital
Hematology
Miscellaneous
Subpart B—Biological Stains
Subpart B—Diagnostic Devices
Subpart C—Cell And Tissue Culture Products
Subpart C—Clinical Laboratory Instruments
Subpart E—Specimen Preparation Reagents
Subpart F—Automated and Semi-Automated Hematology Devices
Subpart F—General Hospital and Personal Use Therapeutic Devices
Subpart F—Immunological Test Systems
Subpart G—Manual Hematology Devices
Subpart G—Tumor Associated Antigen immunological Test Systems
Subpart H—Hematology Kits and Packages
Subpart I—Hematology Reagents
GIR
Reagent, Russel Viper Venom
GJN
Fluid, Diluting, Red-Cell
GJP
Control, Platelet
GJR
Control, Red-Cell
GFS
Standards And Controls, Hemoglobin, Normal And Abnormal
GGJ
Fluid, Diluting, White-Cell
GGK
Products, Red-Cell Lysing Products
GGL
Control, White-Cell
GGM
Control, Hemoglobin
GIF
Diluent, Blood Cell
GLK
Control, Hematocrit
GLQ
Mixture, Control, White-Cell And Red-Cell Indices
JCF
Lymphocyte Separation Medium
K
91
1731
LEUCOPREP(R) BRAND CELL SEPARAT TUBE W/SODIUM CITR
K
90
2445
LYMPHO SEP(TM)
K
89
1407
LEUCOPREP CELL SEPARATION TUBE
K
87
4328
L-PHENYLALANINE METHYL ESTER HYDROCHLORIDE PME REA
K
87
3185
DYNABEADS HLA CELL PREP II ISOLATION PRODUCT
K
87
2775
LEUCOPREP BRAND TUBE
K
86
0354
SEPRACELL LYMPHOCYTE SEPARATION MEDIUM
K
85
4093
LEUCO PREP
K
84
2818
CST
K
84
2146
HISTOPAQUE-1077
Show All 12 Submissions
JCG
Fluid, Diluting, Manual Cell
JCN
Control, Cell Counter, Normal And Abnormal
JCO
Bothrops Atrox Reagent
JPK
Mixture, Hematology Quality Control
KRX
Calibrator For Cell Indices
KRY
Calibrator For Platelet Counting
KRZ
Calibrator For Hemoglobin And Hematocrit Measurement
KSA
Calibrator For Red-Cell And White-Cell Counting
MZG
Test, Residual, Wbc In Leukoreduced Blood
NRF
Material, Quality Control, Semen Analysis
NRS
Control Material, Blood Circulating Epithelial Cancer Cell
Subpart J—Products Used In Establishments That Manufacture Blood and Blood Products
Subpart K—Products Used In Establishments That Manufacture Human Cells, Tissues, and Cellular and Tissue-Based Products (HCT/Ps)
Immunology
Microbiology
Neurology
Obstetrical and Gynecological
Ophthalmic
Orthopedic
Pathology
Physical Medicine
Radiology
General and Plastic Surgery
Toxicology
Medical Genetics
Unknown
HE
/
subpart-i—hematology-reagents
/
JCF
/
K902445
View Source
LYMPHO SEP(TM)
Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K902445
510(k) Type
Traditional
Applicant
ICN BIOMEDICALS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/22/1990
Days to Decision
82 days