FDA Browser
by
Innolitics
Anesthesiology
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
Neurology
Review Panel
Obstetrical and Gynecological
Review Panel
Ophthalmic
Review Panel
Orthopedic
Review Panel
Pathology
Review Panel
Miscellaneous
Miscellaneous
Subpart B—Biological Stains
CFR Sub-Part
Subpart C—Cell And Tissue Culture Products
CFR Sub-Part
Subpart D—Pathology Instrumentation and Accessories
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
Subpart F—Immunological Test Systems
CFR Sub-Part
DEP
Lambda, Peroxidase, Antigen, Antiserum, Control
2
Product Code
DEY
Igm, Peroxidase, Antigen, Antiserum, Control
2
Product Code
DFD
Kappa, Peroxidase, Antigen, Antiserum, Control
2
Product Code
DGH
Igd, Peroxidase, Antigen, Antiserum, Control
2
Product Code
DAA
Igg, Peroxidase, Antigen, Antiserum, Control
2
Product Code
DGO
Ige, Peroxidase, Antigen, Antiserum, Control
2
Product Code
DHF
D/Km-1, Antigen, Antiserum, Control
1
Product Code
LYE
Cytokeratins
2
Product Code
NUA
System, Cystic Fibrosis Transmembrane Conductance Regulator, Gene Mutation Detection
2
Product Code
K
16
3347
xTAG Cystic Fibrosis 39 Kit v2
2
Cleared 510(K)
K
16
3336
xTAG Cystic Fibrosis 60 Kit v2, xTAG Data Analysis Software (TDAS) CFTR
2
Cleared 510(K)
K
08
3845
XTAG CF60 KIT V2
2
Cleared 510(K)
K
08
3846
XTAG CYSTIC FIBROSIS 39 KIT V2, (CFTR 39 KIT V2), MODEL I027C0231, I027D0266, I027E0267
2
Cleared 510(K)
K
08
3294
VERIGENE CFTR NUCLEIC ACID TEST AND VERIGENE CFTR POLYT NUCLEIC ACID TEST
2
Cleared 510(K)
K
09
0901
ESENSOR CF GENOTYPING TESTM ESENSOR SYSTEM, ESENSOR CYSTIC FIBROSIS GENOTYPING TEST, ESENSOR INSTRUMENT, MODELS XT-8
2
Cleared 510(K)
K
06
3787
INPLEX CF MOLECULAR TEST
2
Cleared 510(K)
K
06
2028
CYSTIC FIBROSIS GENOTYPING ASSAY, MODEL 6L20-01
2
Cleared 510(K)
K
06
0627
TAG-IT CYSTIC FIBROSIS KIT
2
Cleared 510(K)
K
06
0543
ESENSOR CYSTIC FIBROSIS CARRIER DETECTION SYSTEM, MODEL ESENSOR 4800
2
Cleared 510(K)
Show All 12 Submissions
PFR
System, Cystic Fibrosis Transmembrane Conductance Regulator Gene, Mutations & Variants Panel Sequencing Detection
2
Product Code
PFS
System, Cystic Fibrosis Transmembrane Conductance Regulator Gene, Variant Gene Sequence Detection
2
Product Code
PKB
Autosomal Recessive Carrier Screening Gene Mutation Detection System
2
Product Code
Subpart G—Tumor Associated Antigen immunological Test Systems
CFR Sub-Part
Subpart H—Hematology Kits and Packages
CFR Sub-Part
Subpart J—Products Used In Establishments That Manufacture Blood and Blood Products
CFR Sub-Part
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 23 May 2025 at 11:06 pm
PA
/
subpart-f—immunological-test-systems
/
NUA
/
K090901
View Source
ESENSOR CF GENOTYPING TESTM ESENSOR SYSTEM, ESENSOR CYSTIC FIBROSIS GENOTYPING TEST, ESENSOR INSTRUMENT, MODELS XT-8
Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K090901
510(k) Type
Traditional
Applicant
OSMETECH MOLECULAR DIAGNOSTICS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/6/2009
Days to Decision
96 days
Submission Type
Summary
FDA Browser
by
Innolitics
Anesthesiology
Cardiovascular
Chemistry
Dental
Ear, Nose, Throat
Gastroenterology and Urology
General Hospital
Hematology
Immunology
Microbiology
Neurology
Obstetrical and Gynecological
Ophthalmic
Orthopedic
Pathology
Miscellaneous
Subpart B—Biological Stains
Subpart C—Cell And Tissue Culture Products
Subpart D—Pathology Instrumentation and Accessories
Subpart E—Immunology Laboratory Equipment and Reagents
Subpart E—Specimen Preparation Reagents
Subpart F—Automated and Semi-Automated Hematology Devices
Subpart F—Immunological Test Systems
DEP
Lambda, Peroxidase, Antigen, Antiserum, Control
DEY
Igm, Peroxidase, Antigen, Antiserum, Control
DFD
Kappa, Peroxidase, Antigen, Antiserum, Control
DGH
Igd, Peroxidase, Antigen, Antiserum, Control
DAA
Igg, Peroxidase, Antigen, Antiserum, Control
DGO
Ige, Peroxidase, Antigen, Antiserum, Control
DHF
D/Km-1, Antigen, Antiserum, Control
LYE
Cytokeratins
NUA
System, Cystic Fibrosis Transmembrane Conductance Regulator, Gene Mutation Detection
K
16
3347
xTAG Cystic Fibrosis 39 Kit v2
K
16
3336
xTAG Cystic Fibrosis 60 Kit v2, xTAG Data Analysis Software (TDAS) CFTR
K
08
3845
XTAG CF60 KIT V2
K
08
3846
XTAG CYSTIC FIBROSIS 39 KIT V2, (CFTR 39 KIT V2), MODEL I027C0231, I027D0266, I027E0267
K
08
3294
VERIGENE CFTR NUCLEIC ACID TEST AND VERIGENE CFTR POLYT NUCLEIC ACID TEST
K
09
0901
ESENSOR CF GENOTYPING TESTM ESENSOR SYSTEM, ESENSOR CYSTIC FIBROSIS GENOTYPING TEST, ESENSOR INSTRUMENT, MODELS XT-8
K
06
3787
INPLEX CF MOLECULAR TEST
K
06
2028
CYSTIC FIBROSIS GENOTYPING ASSAY, MODEL 6L20-01
K
06
0627
TAG-IT CYSTIC FIBROSIS KIT
K
06
0543
ESENSOR CYSTIC FIBROSIS CARRIER DETECTION SYSTEM, MODEL ESENSOR 4800
Show All 12 Submissions
PFR
System, Cystic Fibrosis Transmembrane Conductance Regulator Gene, Mutations & Variants Panel Sequencing Detection
PFS
System, Cystic Fibrosis Transmembrane Conductance Regulator Gene, Variant Gene Sequence Detection
PKB
Autosomal Recessive Carrier Screening Gene Mutation Detection System
Subpart G—Tumor Associated Antigen immunological Test Systems
Subpart H—Hematology Kits and Packages
Subpart J—Products Used In Establishments That Manufacture Blood and Blood Products
Physical Medicine
Radiology
General and Plastic Surgery
Toxicology
Medical Genetics
Unknown
PA
/
subpart-f—immunological-test-systems
/
NUA
/
K090901
View Source
ESENSOR CF GENOTYPING TESTM ESENSOR SYSTEM, ESENSOR CYSTIC FIBROSIS GENOTYPING TEST, ESENSOR INSTRUMENT, MODELS XT-8
Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K090901
510(k) Type
Traditional
Applicant
OSMETECH MOLECULAR DIAGNOSTICS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/6/2009
Days to Decision
96 days
Submission Type
Summary