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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
GKG
Centrifuge, Hematocrit
2
Product Code
GKM
Hand-Tally, Differential
1
Product Code
GJG
Pipette, Quantitative, Hematology
1
Product Code
GJW
Pipette, Pasteur
1
Product Code
GKE
Osmotic Fragility Testing
1
Product Code
GGG
Guaiac Reagent
2
Product Code
GGX
Pipette, Sahli
1
Product Code
GGY
Pipette, Diluting
1
Product Code
GHC
Tube, Sedimentation Rate
1
Product Code
GHO
Hemocytometer
1
Product Code
GHY
Hematocrit, Tube, Rack, Sealer, Holder
2
Product Code
GIO
Tube, Collection, Capillary Blood
1
Product Code
GKW
Aggregometer, Platelet, Thrombokinetogram
2
Product Code
GLG
Platelet Counting, Manual
1
Product Code
JBX
Aggregrometer, Platelet
2
Product Code
JBY
Aggregometer, Platelet, Photo-Optical Scanning
2
Product Code
JBZ
Study, Platelet Adhesive
2
Product Code
JCA
Device, Bleeding Time
2
Product Code
JIO
Blood, Occult, Colorimetric, In Urine
2
Product Code
JIP
Blood, Occult, Enzymatic Method, In Urine
2
Product Code
JPH
Test, Erythrocyte Sedimentation Rate
1
Product Code
JPI
Device, Hematocrit Measuring
2
Product Code
KHE
Reagent, Occult Blood
2
Product Code
OOX
Automated Occult Blood Analyzer
2
Product Code
K
20
0754
Hemosure Accu-Reader A100
2
Cleared 510(K)
K
19
1147
OC-Auto SENSOR io iFOB Test
2
Cleared 510(K)
K
16
3225
AFIAS iFOB with AFIAS-50
2
Cleared 510(K)
K
13
2167
I-CHROMA IFOB WITH I-CHROMA READER
2
Cleared 510(K)
K
09
2330
OC-SENSOR DIANA IFOB TEST
2
Cleared 510(K)
K
04
1408
POLYMEDCO OC AUTO MICRO 80 FOB TEST
2
Cleared 510(K)
OSL
Control, Fecal Occult Blood
2
Product Code
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
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
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Physical Medicine
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Radiology
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General and Plastic Surgery
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Medical Genetics
Review Panel
Unknown
Review Panel
Last synced on 25 April 2025 at 11:05 pm
HE
/
subpart-g—manual-hematology-devices
/
OOX
/
K200754
View Source
Hemosure Accu-Reader A100
Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K200754
510(k) Type
Traditional
Applicant
W.H.P.M., Inc
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/2/2022
Days to Decision
801 days
Submission Type
Summary
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
GKG
Centrifuge, Hematocrit
GKM
Hand-Tally, Differential
GJG
Pipette, Quantitative, Hematology
GJW
Pipette, Pasteur
GKE
Osmotic Fragility Testing
GGG
Guaiac Reagent
GGX
Pipette, Sahli
GGY
Pipette, Diluting
GHC
Tube, Sedimentation Rate
GHO
Hemocytometer
GHY
Hematocrit, Tube, Rack, Sealer, Holder
GIO
Tube, Collection, Capillary Blood
GKW
Aggregometer, Platelet, Thrombokinetogram
GLG
Platelet Counting, Manual
JBX
Aggregrometer, Platelet
JBY
Aggregometer, Platelet, Photo-Optical Scanning
JBZ
Study, Platelet Adhesive
JCA
Device, Bleeding Time
JIO
Blood, Occult, Colorimetric, In Urine
JIP
Blood, Occult, Enzymatic Method, In Urine
JPH
Test, Erythrocyte Sedimentation Rate
JPI
Device, Hematocrit Measuring
KHE
Reagent, Occult Blood
OOX
Automated Occult Blood Analyzer
K
20
0754
Hemosure Accu-Reader A100
K
19
1147
OC-Auto SENSOR io iFOB Test
K
16
3225
AFIAS iFOB with AFIAS-50
K
13
2167
I-CHROMA IFOB WITH I-CHROMA READER
K
09
2330
OC-SENSOR DIANA IFOB TEST
K
04
1408
POLYMEDCO OC AUTO MICRO 80 FOB TEST
OSL
Control, Fecal Occult Blood
Subpart G—Tumor Associated Antigen immunological Test Systems
Subpart H—Hematology Kits and Packages
Subpart I—Hematology Reagents
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-g—manual-hematology-devices
/
OOX
/
K200754
View Source
Hemosure Accu-Reader A100
Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K200754
510(k) Type
Traditional
Applicant
W.H.P.M., Inc
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/2/2022
Days to Decision
801 days
Submission Type
Summary