Anesthesiology
Review Panel
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- General HospitalReview Panel
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- MiscellaneousMiscellaneous
- Subpart B—Biological StainsCFR Sub-Part
- Subpart C—Cell And Tissue Culture ProductsCFR Sub-Part
- Subpart D—Pathology Instrumentation and AccessoriesCFR Sub-Part
- Subpart E—Immunology Laboratory Equipment and ReagentsCFR Sub-Part
- Subpart E—Specimen Preparation ReagentsCFR Sub-Part
- Subpart F—Automated and Semi-Automated Hematology DevicesCFR Sub-Part
- Subpart F—Immunological Test SystemsCFR Sub-Part
- Subpart G—Tumor Associated Antigen immunological Test SystemsCFR Sub-Part
- NQISystem, Immunomagnetic, Circulating Cancer Cell, Enumeration2Product Code
- K130794CELLTRACKS ANALYZER II SYSTEM2Cleared 510(K)
- K122821CELLTRACKS AUTOPREP SYSTEM2Cleared 510(K)
- K110406CELLTRACKS AUTOPREP SYSTEM2Cleared 510(K)
- K113181CELLTRACKS ANALYER II2Cleared 510(K)
- K103502CELLSEARCH CIRCULATING TUMOR CELL KIT MODEL 79000012Cleared 510(K)
- K073338CELLSEARCH CIRCULATING TUMOR CELL KIT2Cleared 510(K)
- K071729CELLSEARCH CIRCULATING TUMOR CELL KIT2Cleared 510(K)
- K062013CELLSEARCH CIRCULATING TUMOR CELL KIT2Cleared 510(K)
- K060110CELLTRACKS ANALYZER II2Cleared 510(K)
- K052191MODIFICATION TO CELLSEARCH CIRCULATING TUMOR CELL KIT2Cleared 510(K)
Show All 13 Submissions
- NYIClassifier, Prognostic, Recurrence Risk Assessment, Rna Gene Expression, Breast Cancer2Product Code
- OVQChronic Lymphocytic Leukemia Fish Probe Kit2Product Code
- OWKEarly Growth Response 1 (Egr) Fish Probe Kit2Product Code
- OWMProstate-Specific Antigen (Psa) For Prognostic, Recurrence Risk Assessment Of Prostate Cancers2Product Code
- OXPDna-Probe Kit, Human Chromosome X And Y, Bmt Engraftment2Product Code
- OYXBcr/Abl1 Monitoring Test2Product Code
- QNCWhole Exome Sequencing Constituent Device2Product Code
- PZMNext Generation Sequencing Based Tumor Profiling Test2Product Code
- QDCDna-Based Test For Minimal Residual Disease For Hematologic Malignancies2Product Code
- Subpart H—Hematology Kits and PackagesCFR Sub-Part
- Subpart J—Products Used In Establishments That Manufacture Blood and Blood ProductsCFR Sub-Part
- Physical MedicineReview Panel
- RadiologyReview Panel
- General and Plastic SurgeryReview Panel
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- Medical GeneticsReview Panel
- UnknownReview Panel
CELLTRACKS AUTOPREP SYSTEM
- Page Type
- Cleared 510(K)
- FDA Hosted PDF* The FDA doesn't provide PDFs for all submissions.
- 510(k) Number
- K110406
- 510(k) Type
- Special
- Applicant
- VERIDEX, LLC
- Country
- United States
- FDA Decision
- Substantially Equivalent
- Decision Date
- 1/20/2012
- Days to Decision
- 340 days
- Submission Type
- Statement