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Review Panel
Cardiovascular
Review Panel
Chemistry
Review Panel
Dental
Review Panel
Ear, Nose, Throat
Review Panel
Gastroenterology and Urology
Review Panel
General Hospital
Review Panel
Hematology
Review Panel
Immunology
Review Panel
Microbiology
Review Panel
Miscellaneous
Miscellaneous
PBK
Non-Variola Orthopoxvirus Real-Time Pcr Primer And Probe Set
2
Product Code
OBF
Assay, Genotyping, Hepatitis C Virus
3
Product Code
QHM
Serology Tests Used For Infectious Disease Screening Of Blood And Plasma Donations
U
Product Code
PRA
Variola Virus Nucleic Acid-Based Detection Assay
2
Product Code
PVQ
Rickettsia Spp. Nucleic Acid Based Detection Assay
2
Product Code
QHO
Nucleic-Acid Tests Used For Infectious Disease Screening Of Blood And Plasma Donations
U
Product Code
QID
Device To Detect Antigens Of Biothreat Microbial Agents In Human Clinical Specimens
2
Product Code
MZP
Assay, Hybridization And/Or Nucleic Acid Amplification For Detection Of Hepatitis C Rna,Hepatitis C Virus
3
Product Code
NCD
Test, Immunity, Cell Mediated, Mycobacterium Tuberculosis
3
Product Code
NWY
Test, Qualitative, Detection Of Dengue Igm And Igg Antibodies
N
Product Code
QPO
Device To Preserve And Stabilize Relative Abundances Of Microbial Nucleic Acids In Clinical Samples
2
Product Code
LOM
Test, Hepatitis B (B Core, Be Antigen, Be Antibody, B Core Igm)
3
Product Code
LQI
Hepatitis Delta Serological Reagents
3
Product Code
MAQ
Kit, Dna Detection, Human Papillomavirus
3
Product Code
MHR
Test, Anti-Tumor Cell Susceptibility
3
Product Code
MKT
Hepatitis Viral B Dna Detection
3
Product Code
MYL
Assay,Enzyme Linked Immunosorbent,Parvovirus B19 Igg
3
Product Code
MYM
Assay,Enzyme Linked Immunosorbent,Parvovirus B19 Igm
3
Product Code
MZO
Assay, Enzyme Linked Immunosorbent, Hepatitis C Virus
3
Product Code
OIH
Yersinia Spp. Reagents
U
Product Code
OJN
Mycobacterium Tuberculosis, Cell Mediated Immune Response, Enzyme-Linked Immunospot Test
3
Product Code
OJO
Enzyme Linked Immunosorbent Assay For The Detection Of Lipoarabinomannan Antigen Of Mycobacteria
N
Product Code
ORL
Whole Blood Pre-Treatment T-Cell Enrichment Reagent
3
Product Code
OTT
Research Use Only/Microbiology
N
Product Code
OYB
Kit, Rna Detection, Human Papillomavirus
3
Product Code
PAB
Cytomegalovirus (Cmv) Dna Quantitative Assay
3
Product Code
PCY
Investigational Use Only - Microbiology
N
Product Code
POA
Reagents, Zika Virus Nucleic Acid
N
Product Code
POG
Reagents, Ebola Zaire Virus (Detected In The West Africa Outbreak In 2014) Nucleic Acid
N
Product Code
PYS
Zika Virus Serological Reagents (Emergency Use)
N
Product Code
QHV
Multiple Osteoarticular Pathogen Antigen Kit
N
Product Code
QIM
Bartonella Spp. Serological Reagents
N
Product Code
QIN
Babesia Spp. Serological Reagents
N
Product Code
QIO
Anaplasma Spp. And Ehrlichia Spp. Serological Reagents
N
Product Code
QIP
Rickettsia Spp. (Spotted Fever Group Or Typhus Group) Serological Reagents
N
Product Code
QIQ
Orientia Spp. (Scrub Typhus) Serological Reagents
N
Product Code
QJR
Reagents, 2019-Novel Coronavirus Nucleic Acid
N
Product Code
QKO
Reagent, Coronavirus Serological
N
Product Code
QKP
Coronavirus Antigen Detection Test System.
N
Product Code
QLT
Covid-19 Multi-Analyte Respiratory Panel Nucleic Acid Devices
N
Product Code
QLW
Covid-19 Test Home Collection Kit Devices
N
Product Code
QMN
Covid-19 Multi-Analyte Antigen Device
N
Product Code
QSH
Coronavirus Marker Detection
N
Product Code
QSN
Orthopedic Infection Microbial Multiplex Nucleic Acid Detection System
2
Product Code
QSS
Hiv Self-Tests
3
Product Code
QTA
Ngs Whole Genome Sequencing For Sars-Cov-2 Genetic Analysis
N
Product Code
QTP
Reagents, Monkeypox Virus Nucleic Acid.
N
Product Code
QTQ
Reagents, Non-Variola Orthopoxvirus Nucleic Acid.
N
Product Code
QWB
Over-The-Counter Molecular Test To Detect Sars-Cov-2 From Clinical Specimens
2
Product Code
QVR
Multiplex Nucleic Acid Detection System For Biothreat Agents
2
Product Code
QUU
Simple In Vitro Diagnostic Device For The Detection Of Secreted Proteins From Bacillus Spp. In Human Clinical Samples
2
Product Code
QVF
Simple Point-Of-Care Device To Directly Detect Sars-Cov-2 Viral Targets From Clinical Specimens In Near-Patient Settings
2
Product Code
QVP
Sars-Cov-2 Serology Test
2
Product Code
QWR
Simple Point-Of-Care Device To Detect Sar-Cov-2 Nucleic Acid Targets From Clinical Specimens In Near-Patient Settings
2
Product Code
QYA
System For Detection Of Nucleic Acid From Non-Viral Microorganism(S) Causing Stis Using Specimens Collected At Home
2
Product Code
QYT
Over-The-Counter Covid-19 Antigen Test
2
Product Code
SBP
Simple Point-Of-Care Nucleic Acid-Based Hepatitis C Virus Ribonucleic Acid Test
2
Product Code
SBT
Device To Detect Microbial Colonization Directly From Clinical Specimens.
2
Product Code
SBZ
Test For Detection Of Antibodies Associated With Syphilis Performed By Lay Users
2
Product Code
SCA
Multi-Analyte Respiratory Virus Antigen Detection Test
2
Product Code
SDM
Nucleic Acid Test Used For Screening Of Cadaveric (Non-Heart-Beating) Donors Of Blood Or Blood Products Or Hct/Ps
U
Product Code
SDN
Serology Test Used For Screening Of Cadaveric (Non-Heart-Beating) Donors Of Blood Or Blood Products Or Hct/Ps
U
Product Code
SEA
Test For Detection Of Microorganism(S) Causing Sexually Transmitted Infections Performed By Lay Users
2
Product Code
SEP
Device For Home Collection And Transport Of Vaginal Specimens By Lay Users For Use In An Approved Hpv Molecular Assay
2
Product Code
SGA
Biothreat Microbial Agent Nucleic Acid Detection Test
2
Product Code
QTU
Reagents, Non-Variola Orthopoxvirus Or Monkeypox Virus Singleplex Antigen Tests
N
Product Code
SGW
Device To Detect Antibodies To Hepatitis D Virus
2
Product Code
Submissions with No Product Code
Miscellaneous
K
24
3730
Xpert C. difficile/Epi
Cleared 510(K)
P
99
0044
DIASORIN ETI-CORE-IGMK PLUS ASSAY
APPR
PMA Approval
P
99
0045
DIASORIN ETI-AB-COREK PLUS ASSAY
APPR
PMA Approval
P
99
0041
DIASORIN ETI-AB-EBK PLUS ASSAY
APPR
PMA Approval
K
87
0171
(MERIFLUOR)TM-CRYPTOSPORIDIUM
Cleared 510(K)
K
85
2976
NEG COMBO PANELS, NEG/URI MIC,NEG ID,POS MIC
Cleared 510(K)
K
85
2423
TIMENTIN 85MCG SENSITIVITY DISC
Cleared 510(K)
K
84
4058
CODE-A-WALL SERIES 1-250 INOCULUM TRAY
Cleared 510(K)
K
84
3770
BIOTIS LYSINE IRON AGAR
Cleared 510(K)
K
84
2400
BIOTIS N.Y.C. CARBOHYDRATE FERMENTA-
Cleared 510(K)
P
99
0041
ETI-AB-EBK PLUS assay
OK30
PMA Approval
P
99
0041
ETI-AB-EBK PLUS assay
OK30
PMA Approval
P
99
0045
ETI-AB-COREK PLUS assay
OK30
PMA Approval
P
99
0044
ETI-CORE-IGMK PLUS assay
OK30
PMA Approval
P
99
0041
ETI-AB-EBK PLUS assay
OK30
PMA Approval
P
99
0044
ETI-CORE-IGMK PLUS assay
OK30
PMA Approval
P
99
0045
ETI-AB-COREK PLUS assay
OK30
PMA Approval
P
99
0044
ETI-CORE-IGMK Plus Assay
OK30
PMA Approval
P
99
0041
ETI-AB-EBK Plus Assay
OK30
PMA Approval
P
99
0045
ETI-AB-COREK Plus Assay
OK30
PMA Approval
P
99
0041
ETI-AB-EBK PLUS Assay
OK30
PMA Approval
P
99
0044
ETI-CORE-IGMK PLUS Assay
OK30
PMA Approval
P
99
0045
ETI-AB-COREK PLUS Assay
OK30
PMA Approval
P
99
0041
ETI-AB-EBK PLUS Assay
OK30
PMA Approval
P
99
0045
ETI-AB-COREK PLUS Assay
OK30
PMA Approval
P
99
0044
ETI-CORE-IGMK PLUS Assay
OK30
PMA Approval
P
99
0044
ETI-CORE-IGMK PLUS Assay
OK30
PMA Approval
P
99
0045
ETI-AB-COREK PLUS Assay
OK30
PMA Approval
P
99
0041
ETI-AB-EBK PLUS Assay
OK30
PMA Approval
P
99
0045
ETI-AB-COREK PLUS assay
OK30
PMA Approval
P
99
0041
ETI-AB-EBK PLUS assay
OK30
PMA Approval
P
99
0044
ETI-CORE-IGMK PLUS assay
OK30
PMA Approval
P
99
0041
DiaSorin ETI-AB-EBK PLUS assay
OK30
PMA Approval
P
99
0044
DiaSorin ETI-CORE-IGMK PLUS assay
OK30
PMA Approval
P
99
0045
DiaSorin ETI-AB-COREK PLUS assay
OK30
PMA Approval
P
99
0045
ETI-AB-COREK PLUS assay
OK30
PMA Approval
P
99
0044
ETI-CORE-IGMK PLUS assay
OK30
PMA Approval
P
99
0041
ETI-AB-EBK PLUS assay
OK30
PMA Approval
P
99
0041
ETI-AB-EBK PLUS ASSAY
OK30
PMA Approval
P
99
0045
ETI-AB-COREK PLUS ASSAY
OK30
PMA Approval
P
99
0044
ETI-CORE-IGMK PLUS ASSAY
OK30
PMA Approval
P
05
0028
COBAS AMPLIPREP/COBAS TAQMAN HBV TEST V2.0
OK30
PMA Approval
P
05
0028
COBAS AMPLIPREP/COBAS TAQMAN HBV TEST
OK30
PMA Approval
P
05
0028
COBAS AMPLIPREP/COBAS TAQMAN HBV TEST V.2.0
OK30
PMA Approval
P
05
0028
COBAS AMPLIPREP/COBAS TAQMAN HBV TEST
OK30
PMA Approval
P
05
0028
COBAS TAQMAN HBV TEST
OK30
PMA Approval
P
05
0028
COBAS TAQMAN HBV TEST FOR USE WITH THE HIGH PURE SYSTEM
OK30
PMA Approval
P
05
0028
COBAS TAQMAN HBV TEST FOR USE WITH THE HIGH PURE SYSTEM
OK30
PMA Approval
P
05
0028
COBAS TAQMAN HBV TEST FOR USE WITH THE HIGH PURE SYSTEM
OK30
PMA Approval
P
05
0028
COBAS TAQMAN HBV TEST
OK30
PMA Approval
P
00
0010
COBAS AMPLICOR HCV TEST, V2.0
OK30
PMA Approval
P
94
0034
GEN-PROBE AMPLIFIED MYCOBACTERIUM TUBERCULOSIS DIRECT TEST
APPR
PMA Approval
P
99
0044
DIASORIN ETI-CORE-IGMK PLUS ASSAY
APPR
PMA Approval
P
99
0045
DIASORIN ETI-AB-COREK PLUS ASSAY
APPR
PMA Approval
P
99
0041
DIASORIN ETI-AB-EBK PLUS ASSAY
APPR
PMA Approval
P
94
0034
GEN-PROBE(R) AMPLIFIED MYCOBACTERIUM TUBERCULOSIS DIRECT TEST (MTD TEST)
APPR
PMA Approval
P
94
0034
GEN-PROBE(R) AMPLIFIED(TM) MYCOBACTERIUM TUBERCULOSIS DIRECT (MTD) TEST
APPR
PMA Approval
P
94
0034
GEN-PROBE(R) AMPLIFIED MYCOBACTERIUM TUBERCULOSIS DIRECT TEST (MTD TEST)
APPR
PMA Approval
P
94
0034
GEN-PROBE AMPLIFIED MYCOBACTERIUM TUBERCULOSIS DIRECT TEST
OK30
PMA Approval
P
94
0034
AMPLIFED MYCOBACTERIUM TUBERCULOSIS DIRECTOR (MTD) TEST
APPR
PMA Approval
P
94
0034
GEN-PROBE(R) AMPLIFIED MYCOBACTERIUM TUBERCULOSIS DIRECT TEST (MTD TEST)
APPR
PMA Approval
K
84
2182
TITERTEK-ENTEROBAC RAPID AUTOMATED
Cleared 510(K)
K
84
1660
SELENITE CYSTINE BROTH BASE
Cleared 510(K)
K
84
1915
PHAMAS ALLERGY MGMT. SYSTEM
Cleared 510(K)
K
84
0851
VIRAL TRANSPORT MEDIUM
Cleared 510(K)
K
83
3292
LACTABACILLUS AGAR W/O TWEEN80
Cleared 510(K)
K
83
3027
HAEMOPHILUS/NEISSERIA IDENTIF-PANEL
Cleared 510(K)
K
83
3214
DEXTROSE
Cleared 510(K)
K
83
2934
MACCONKEY'S AGAR PLATE
Cleared 510(K)
K
83
0646
DIRECTIGEN NEISSERIA MENINGITIDIS
Cleared 510(K)
K
82
2518
CSM BETA-LACTAMASE DISC
Cleared 510(K)
K
82
0208
ZYME A
Cleared 510(K)
K
81
2123
CYTOMEGELISA TEST KIT
Cleared 510(K)
K
80
0052
ANTIMICROBIAL REMOVAL DEVICE (ARD)
Cleared 510(K)
K
78
1283
READER, INOCULUM, STDIZED.
Cleared 510(K)
K
78
1097
INOCULUM STDIZING SYS., INOCUPAC
Cleared 510(K)
K
78
0114
IMMUNOZYME E. HISTOLYTICA ANTIGENS
Cleared 510(K)
K
77
1569
AUTOSTREAKER
Cleared 510(K)
K
76
0356
DISH, STERILE DISPOSABLE POLYSTYRENE
Cleared 510(K)
K
76
0583
DISPOSABLE/BOROSILICATE CULTURE TUBES
Cleared 510(K)
N
17
578
INDIRECT FLUORESCENT-ANTIBODY TEST FOR GONORRHEA (IFA-GC)
APPR
PMA Approval
Subpart B—Biological Stains
CFR Sub-Part
Subpart B—Clinical Chemistry Test Systems
CFR Sub-Part
Subpart B—Diagnostic Devices
CFR Sub-Part
Subpart C—Clinical Laboratory Instruments
CFR Sub-Part
Subpart C—Microbiology Devices
CFR Sub-Part
Subpart D—Serological Reagents
CFR Sub-Part
Subpart F—Immunological Test Systems
CFR Sub-Part
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 25 January 2026 at 3:41 am
MI
/
MI-misc
/
no-product-code
/
K830646
View Source
DIRECTIGEN NEISSERIA MENINGITIDIS
Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
PDF
Analyzed PDF
510(k) Number
K830646
510(k) Type
Traditional
Applicant
BD BECTON DICKINSON VACUTAINER SYSTEMS PREANALYTIC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/27/1983
Days to Decision
87 days
FDA Browser
by
Innolitics
Anesthesiology
Cardiovascular
Chemistry
Dental
Ear, Nose, Throat
Gastroenterology and Urology
General Hospital
Hematology
Immunology
Microbiology
Miscellaneous
PBK
Non-Variola Orthopoxvirus Real-Time Pcr Primer And Probe Set
OBF
Assay, Genotyping, Hepatitis C Virus
QHM
Serology Tests Used For Infectious Disease Screening Of Blood And Plasma Donations
PRA
Variola Virus Nucleic Acid-Based Detection Assay
PVQ
Rickettsia Spp. Nucleic Acid Based Detection Assay
QHO
Nucleic-Acid Tests Used For Infectious Disease Screening Of Blood And Plasma Donations
QID
Device To Detect Antigens Of Biothreat Microbial Agents In Human Clinical Specimens
MZP
Assay, Hybridization And/Or Nucleic Acid Amplification For Detection Of Hepatitis C Rna,Hepatitis C Virus
NCD
Test, Immunity, Cell Mediated, Mycobacterium Tuberculosis
NWY
Test, Qualitative, Detection Of Dengue Igm And Igg Antibodies
QPO
Device To Preserve And Stabilize Relative Abundances Of Microbial Nucleic Acids In Clinical Samples
LOM
Test, Hepatitis B (B Core, Be Antigen, Be Antibody, B Core Igm)
LQI
Hepatitis Delta Serological Reagents
MAQ
Kit, Dna Detection, Human Papillomavirus
MHR
Test, Anti-Tumor Cell Susceptibility
MKT
Hepatitis Viral B Dna Detection
MYL
Assay,Enzyme Linked Immunosorbent,Parvovirus B19 Igg
MYM
Assay,Enzyme Linked Immunosorbent,Parvovirus B19 Igm
MZO
Assay, Enzyme Linked Immunosorbent, Hepatitis C Virus
OIH
Yersinia Spp. Reagents
OJN
Mycobacterium Tuberculosis, Cell Mediated Immune Response, Enzyme-Linked Immunospot Test
OJO
Enzyme Linked Immunosorbent Assay For The Detection Of Lipoarabinomannan Antigen Of Mycobacteria
ORL
Whole Blood Pre-Treatment T-Cell Enrichment Reagent
OTT
Research Use Only/Microbiology
OYB
Kit, Rna Detection, Human Papillomavirus
PAB
Cytomegalovirus (Cmv) Dna Quantitative Assay
PCY
Investigational Use Only - Microbiology
POA
Reagents, Zika Virus Nucleic Acid
POG
Reagents, Ebola Zaire Virus (Detected In The West Africa Outbreak In 2014) Nucleic Acid
PYS
Zika Virus Serological Reagents (Emergency Use)
QHV
Multiple Osteoarticular Pathogen Antigen Kit
QIM
Bartonella Spp. Serological Reagents
QIN
Babesia Spp. Serological Reagents
QIO
Anaplasma Spp. And Ehrlichia Spp. Serological Reagents
QIP
Rickettsia Spp. (Spotted Fever Group Or Typhus Group) Serological Reagents
QIQ
Orientia Spp. (Scrub Typhus) Serological Reagents
QJR
Reagents, 2019-Novel Coronavirus Nucleic Acid
QKO
Reagent, Coronavirus Serological
QKP
Coronavirus Antigen Detection Test System.
QLT
Covid-19 Multi-Analyte Respiratory Panel Nucleic Acid Devices
QLW
Covid-19 Test Home Collection Kit Devices
QMN
Covid-19 Multi-Analyte Antigen Device
QSH
Coronavirus Marker Detection
QSN
Orthopedic Infection Microbial Multiplex Nucleic Acid Detection System
QSS
Hiv Self-Tests
QTA
Ngs Whole Genome Sequencing For Sars-Cov-2 Genetic Analysis
QTP
Reagents, Monkeypox Virus Nucleic Acid.
QTQ
Reagents, Non-Variola Orthopoxvirus Nucleic Acid.
QWB
Over-The-Counter Molecular Test To Detect Sars-Cov-2 From Clinical Specimens
QVR
Multiplex Nucleic Acid Detection System For Biothreat Agents
QUU
Simple In Vitro Diagnostic Device For The Detection Of Secreted Proteins From Bacillus Spp. In Human Clinical Samples
QVF
Simple Point-Of-Care Device To Directly Detect Sars-Cov-2 Viral Targets From Clinical Specimens In Near-Patient Settings
QVP
Sars-Cov-2 Serology Test
QWR
Simple Point-Of-Care Device To Detect Sar-Cov-2 Nucleic Acid Targets From Clinical Specimens In Near-Patient Settings
QYA
System For Detection Of Nucleic Acid From Non-Viral Microorganism(S) Causing Stis Using Specimens Collected At Home
QYT
Over-The-Counter Covid-19 Antigen Test
SBP
Simple Point-Of-Care Nucleic Acid-Based Hepatitis C Virus Ribonucleic Acid Test
SBT
Device To Detect Microbial Colonization Directly From Clinical Specimens.
SBZ
Test For Detection Of Antibodies Associated With Syphilis Performed By Lay Users
SCA
Multi-Analyte Respiratory Virus Antigen Detection Test
SDM
Nucleic Acid Test Used For Screening Of Cadaveric (Non-Heart-Beating) Donors Of Blood Or Blood Products Or Hct/Ps
SDN
Serology Test Used For Screening Of Cadaveric (Non-Heart-Beating) Donors Of Blood Or Blood Products Or Hct/Ps
SEA
Test For Detection Of Microorganism(S) Causing Sexually Transmitted Infections Performed By Lay Users
SEP
Device For Home Collection And Transport Of Vaginal Specimens By Lay Users For Use In An Approved Hpv Molecular Assay
SGA
Biothreat Microbial Agent Nucleic Acid Detection Test
QTU
Reagents, Non-Variola Orthopoxvirus Or Monkeypox Virus Singleplex Antigen Tests
SGW
Device To Detect Antibodies To Hepatitis D Virus
Submissions with No Product Code
K
24
3730
Xpert C. difficile/Epi
P
99
0044
DIASORIN ETI-CORE-IGMK PLUS ASSAY
P
99
0045
DIASORIN ETI-AB-COREK PLUS ASSAY
P
99
0041
DIASORIN ETI-AB-EBK PLUS ASSAY
K
87
0171
(MERIFLUOR)TM-CRYPTOSPORIDIUM
K
85
2976
NEG COMBO PANELS, NEG/URI MIC,NEG ID,POS MIC
K
85
2423
TIMENTIN 85MCG SENSITIVITY DISC
K
84
4058
CODE-A-WALL SERIES 1-250 INOCULUM TRAY
K
84
3770
BIOTIS LYSINE IRON AGAR
K
84
2400
BIOTIS N.Y.C. CARBOHYDRATE FERMENTA-
P
99
0041
ETI-AB-EBK PLUS assay
P
99
0041
ETI-AB-EBK PLUS assay
P
99
0045
ETI-AB-COREK PLUS assay
P
99
0044
ETI-CORE-IGMK PLUS assay
P
99
0041
ETI-AB-EBK PLUS assay
P
99
0044
ETI-CORE-IGMK PLUS assay
P
99
0045
ETI-AB-COREK PLUS assay
P
99
0044
ETI-CORE-IGMK Plus Assay
P
99
0041
ETI-AB-EBK Plus Assay
P
99
0045
ETI-AB-COREK Plus Assay
P
99
0041
ETI-AB-EBK PLUS Assay
P
99
0044
ETI-CORE-IGMK PLUS Assay
P
99
0045
ETI-AB-COREK PLUS Assay
P
99
0041
ETI-AB-EBK PLUS Assay
P
99
0045
ETI-AB-COREK PLUS Assay
P
99
0044
ETI-CORE-IGMK PLUS Assay
P
99
0044
ETI-CORE-IGMK PLUS Assay
P
99
0045
ETI-AB-COREK PLUS Assay
P
99
0041
ETI-AB-EBK PLUS Assay
P
99
0045
ETI-AB-COREK PLUS assay
P
99
0041
ETI-AB-EBK PLUS assay
P
99
0044
ETI-CORE-IGMK PLUS assay
P
99
0041
DiaSorin ETI-AB-EBK PLUS assay
P
99
0044
DiaSorin ETI-CORE-IGMK PLUS assay
P
99
0045
DiaSorin ETI-AB-COREK PLUS assay
P
99
0045
ETI-AB-COREK PLUS assay
P
99
0044
ETI-CORE-IGMK PLUS assay
P
99
0041
ETI-AB-EBK PLUS assay
P
99
0041
ETI-AB-EBK PLUS ASSAY
P
99
0045
ETI-AB-COREK PLUS ASSAY
P
99
0044
ETI-CORE-IGMK PLUS ASSAY
P
05
0028
COBAS AMPLIPREP/COBAS TAQMAN HBV TEST V2.0
P
05
0028
COBAS AMPLIPREP/COBAS TAQMAN HBV TEST
P
05
0028
COBAS AMPLIPREP/COBAS TAQMAN HBV TEST V.2.0
P
05
0028
COBAS AMPLIPREP/COBAS TAQMAN HBV TEST
P
05
0028
COBAS TAQMAN HBV TEST
P
05
0028
COBAS TAQMAN HBV TEST FOR USE WITH THE HIGH PURE SYSTEM
P
05
0028
COBAS TAQMAN HBV TEST FOR USE WITH THE HIGH PURE SYSTEM
P
05
0028
COBAS TAQMAN HBV TEST FOR USE WITH THE HIGH PURE SYSTEM
P
05
0028
COBAS TAQMAN HBV TEST
P
00
0010
COBAS AMPLICOR HCV TEST, V2.0
P
94
0034
GEN-PROBE AMPLIFIED MYCOBACTERIUM TUBERCULOSIS DIRECT TEST
P
99
0044
DIASORIN ETI-CORE-IGMK PLUS ASSAY
P
99
0045
DIASORIN ETI-AB-COREK PLUS ASSAY
P
99
0041
DIASORIN ETI-AB-EBK PLUS ASSAY
P
94
0034
GEN-PROBE(R) AMPLIFIED MYCOBACTERIUM TUBERCULOSIS DIRECT TEST (MTD TEST)
P
94
0034
GEN-PROBE(R) AMPLIFIED(TM) MYCOBACTERIUM TUBERCULOSIS DIRECT (MTD) TEST
P
94
0034
GEN-PROBE(R) AMPLIFIED MYCOBACTERIUM TUBERCULOSIS DIRECT TEST (MTD TEST)
P
94
0034
GEN-PROBE AMPLIFIED MYCOBACTERIUM TUBERCULOSIS DIRECT TEST
P
94
0034
AMPLIFED MYCOBACTERIUM TUBERCULOSIS DIRECTOR (MTD) TEST
P
94
0034
GEN-PROBE(R) AMPLIFIED MYCOBACTERIUM TUBERCULOSIS DIRECT TEST (MTD TEST)
K
84
2182
TITERTEK-ENTEROBAC RAPID AUTOMATED
K
84
1660
SELENITE CYSTINE BROTH BASE
K
84
1915
PHAMAS ALLERGY MGMT. SYSTEM
K
84
0851
VIRAL TRANSPORT MEDIUM
K
83
3292
LACTABACILLUS AGAR W/O TWEEN80
K
83
3027
HAEMOPHILUS/NEISSERIA IDENTIF-PANEL
K
83
3214
DEXTROSE
K
83
2934
MACCONKEY'S AGAR PLATE
K
83
0646
DIRECTIGEN NEISSERIA MENINGITIDIS
K
82
2518
CSM BETA-LACTAMASE DISC
K
82
0208
ZYME A
K
81
2123
CYTOMEGELISA TEST KIT
K
80
0052
ANTIMICROBIAL REMOVAL DEVICE (ARD)
K
78
1283
READER, INOCULUM, STDIZED.
K
78
1097
INOCULUM STDIZING SYS., INOCUPAC
K
78
0114
IMMUNOZYME E. HISTOLYTICA ANTIGENS
K
77
1569
AUTOSTREAKER
K
76
0356
DISH, STERILE DISPOSABLE POLYSTYRENE
K
76
0583
DISPOSABLE/BOROSILICATE CULTURE TUBES
N
17
578
INDIRECT FLUORESCENT-ANTIBODY TEST FOR GONORRHEA (IFA-GC)
Subpart B—Biological Stains
Subpart B—Clinical Chemistry Test Systems
Subpart B—Diagnostic Devices
Subpart C—Clinical Laboratory Instruments
Subpart C—Microbiology Devices
Subpart D—Serological Reagents
Subpart F—Immunological Test Systems
Neurology
Obstetrical and Gynecological
Ophthalmic
Orthopedic
Pathology
Physical Medicine
Radiology
General and Plastic Surgery
Toxicology
Medical Genetics
Unknown
MI
/
MI-misc
/
no-product-code
/
K830646
View Source
DIRECTIGEN NEISSERIA MENINGITIDIS
Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
PDF
Analyzed PDF
510(k) Number
K830646
510(k) Type
Traditional
Applicant
BD BECTON DICKINSON VACUTAINER SYSTEMS PREANALYTIC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/27/1983
Days to Decision
87 days