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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
GKF
Instrument, Hematocrit, Automated
2
Product Code
GKH
Apparatus, Automated Blood Cell Diluting
1
Product Code
GKJ
Spinner, Slide, Automated
1
Product Code
GKL
Counter, Cell, Automated (Particle Counter)
2
Product Code
GKN
Timer, Clot, Automated
2
Product Code
GIZ
Plasma, Control, Normal
2
Product Code
GKB
Device, Automated Sedimentation Rate
1
Product Code
GGC
Control, Plasma, Abnormal
2
Product Code
GGN
Plasma, Coagulation Control
2
Product Code
GHK
Centrifuge, Microsedimentation
1
Product Code
GHR
Reagent, Platelet Aggregation
2
Product Code
GIE
Fibrometer
2
Product Code
GKP
Instrument, Coagulation, Automated
2
Product Code
GKR
System, Hemoglobin, Automated
2
Product Code
GKX
Instrument, Automated Platelet Counting
2
Product Code
GKZ
Counter, Differential Cell
2
Product Code
JBT
Timer, Coagulation
2
Product Code
JBW
Red-Cell Indices, Measured
2
Product Code
JOX
Analyzer, Heparin, Automated
2
Product Code
JOY
Device, Automated Cell-Locating
2
Product Code
JOZ
System, Automated Platelet Aggregation
2
Product Code
JPA
System, Multipurpose For In Vitro Coagulation Studies
2
Product Code
JPJ
Red-Cell Indices, Calculated
2
Product Code
JWO
Device, Blood Volume Measuring
2
Product Code
KQG
Instrument, Coagulation
2
Product Code
KQH
Red-Cell Indices
2
Product Code
LGP
Assay, Alpha-2-Antiplasmin
2
Product Code
LKM
Counter, Urine Particle
2
Product Code
LLG
Kit, Igg, Platelet Associated
2
Product Code
MAM
Dna-Probe, B And T Lymphocyte
2
Product Code
OBW
11-Dehydro Thromboxane B2 Kit, Urinary
2
Product Code
OYE
Flow Cytometric Reagents And Accessories.
2
Product Code
PMG
Automated Multicolor Fluorescent Imaging Cytometric Analysis System
2
Product Code
POV
Semen Analysis Device
2
Product Code
K
24
1628
YO Home Sperm Test
2
Cleared 510(K)
K
22
0828
SQA-iO Sperm Quality Analyzer
2
Cleared 510(K)
K
20
2089
LensHooke X1 PRO Semen Quality Analyzer, LensHooke X1 PRO SE Semen Quality Analyzer
2
Cleared 510(K)
K
18
3602
SwimCount Sperm Quality Test
2
Cleared 510(K)
K
18
0343
LensHooke X1 Pro Semen Quality Analyzer, LensHooke X1 Semen Quality Analyzer
2
Cleared 510(K)
K
17
2514
Trak Plus Male Fertility Testing System
2
Cleared 510(K)
K
16
1493
YO Home Sperm Test
2
Cleared 510(K)
K
15
3683
Trak Male Fertility Testing System
2
Cleared 510(K)
K
10
0341
SPERMCHECK FERTILITY
2
Cleared 510(K)
K
07
3039
SPERMCHECK VASECTOMY
2
Cleared 510(K)
K
07
1737
GENERAL SEMEN ANALYSIS KIT
2
Cleared 510(K)
K
06
3864
QWIKCHECK TEST STRIPS- REAGENT STRIPS FOR SEMEN ANALYSIS
2
Cleared 510(K)
K
04
1039
FERTELL MALE FERTILITY TEST
2
Cleared 510(K)
K
03
2874
HBA SPERM-HYALURONAN BINDING ASSAY
2
Cleared 510(K)
K
02
4337
GENERAL SEMEN ANALYSIS (GSA) KIT
2
Cleared 510(K)
K
02
1746
SQA V, SPERM QUALITY ANALYZER
2
Cleared 510(K)
K
01
2805
AUTOMARQER
2
Cleared 510(K)
K
01
2352
SQA, SPERM QUALITY ANALYZER
2
Cleared 510(K)
K
01
1679
FERTILMARQ HOME DIAGNOSTIC SCREENING TEST KIT FOR MALE INFERTILITY
2
Cleared 510(K)
K
99
0184
AUTOMARQER
2
Cleared 510(K)
K
98
3473
FERTILMARQ TEST KIT
2
Cleared 510(K)
K
91
5229
SEMEN ANALYSIS KIT
2
Cleared 510(K)
K
89
4949
SQA
2
Cleared 510(K)
K
88
1765
CTS-3060 AUTOMATED SEMEN ANALYZER
2
Cleared 510(K)
QFR
Coagulation System For The Measurement Of Whole Blood Viscoelastic Properties
2
Product Code
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
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
Medical Genetics
Review Panel
Unknown
Review Panel
Last synced on 16 May 2025 at 11:05 pm
HE
/
subpart-f—automated-and-semi-automated-hematology-devices
/
POV
/
K894949
View Source
SQA
Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K894949
510(k) Type
Traditional
Applicant
UNITED MEDICAL SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/29/1989
Days to Decision
148 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
GKF
Instrument, Hematocrit, Automated
GKH
Apparatus, Automated Blood Cell Diluting
GKJ
Spinner, Slide, Automated
GKL
Counter, Cell, Automated (Particle Counter)
GKN
Timer, Clot, Automated
GIZ
Plasma, Control, Normal
GKB
Device, Automated Sedimentation Rate
GGC
Control, Plasma, Abnormal
GGN
Plasma, Coagulation Control
GHK
Centrifuge, Microsedimentation
GHR
Reagent, Platelet Aggregation
GIE
Fibrometer
GKP
Instrument, Coagulation, Automated
GKR
System, Hemoglobin, Automated
GKX
Instrument, Automated Platelet Counting
GKZ
Counter, Differential Cell
JBT
Timer, Coagulation
JBW
Red-Cell Indices, Measured
JOX
Analyzer, Heparin, Automated
JOY
Device, Automated Cell-Locating
JOZ
System, Automated Platelet Aggregation
JPA
System, Multipurpose For In Vitro Coagulation Studies
JPJ
Red-Cell Indices, Calculated
JWO
Device, Blood Volume Measuring
KQG
Instrument, Coagulation
KQH
Red-Cell Indices
LGP
Assay, Alpha-2-Antiplasmin
LKM
Counter, Urine Particle
LLG
Kit, Igg, Platelet Associated
MAM
Dna-Probe, B And T Lymphocyte
OBW
11-Dehydro Thromboxane B2 Kit, Urinary
OYE
Flow Cytometric Reagents And Accessories.
PMG
Automated Multicolor Fluorescent Imaging Cytometric Analysis System
POV
Semen Analysis Device
K
24
1628
YO Home Sperm Test
K
22
0828
SQA-iO Sperm Quality Analyzer
K
20
2089
LensHooke X1 PRO Semen Quality Analyzer, LensHooke X1 PRO SE Semen Quality Analyzer
K
18
3602
SwimCount Sperm Quality Test
K
18
0343
LensHooke X1 Pro Semen Quality Analyzer, LensHooke X1 Semen Quality Analyzer
K
17
2514
Trak Plus Male Fertility Testing System
K
16
1493
YO Home Sperm Test
K
15
3683
Trak Male Fertility Testing System
K
10
0341
SPERMCHECK FERTILITY
K
07
3039
SPERMCHECK VASECTOMY
K
07
1737
GENERAL SEMEN ANALYSIS KIT
K
06
3864
QWIKCHECK TEST STRIPS- REAGENT STRIPS FOR SEMEN ANALYSIS
K
04
1039
FERTELL MALE FERTILITY TEST
K
03
2874
HBA SPERM-HYALURONAN BINDING ASSAY
K
02
4337
GENERAL SEMEN ANALYSIS (GSA) KIT
K
02
1746
SQA V, SPERM QUALITY ANALYZER
K
01
2805
AUTOMARQER
K
01
2352
SQA, SPERM QUALITY ANALYZER
K
01
1679
FERTILMARQ HOME DIAGNOSTIC SCREENING TEST KIT FOR MALE INFERTILITY
K
99
0184
AUTOMARQER
K
98
3473
FERTILMARQ TEST KIT
K
91
5229
SEMEN ANALYSIS KIT
K
89
4949
SQA
K
88
1765
CTS-3060 AUTOMATED SEMEN ANALYZER
QFR
Coagulation System For The Measurement Of Whole Blood Viscoelastic Properties
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
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-f—automated-and-semi-automated-hematology-devices
/
POV
/
K894949
View Source
SQA
Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K894949
510(k) Type
Traditional
Applicant
UNITED MEDICAL SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/29/1989
Days to Decision
148 days