Anesthesiology
Review Panel
- CardiovascularReview Panel
- ChemistryReview Panel
- DentalReview Panel
- Ear, Nose, ThroatReview Panel
- Gastroenterology and UrologyReview Panel
- General HospitalReview Panel
- HematologyReview Panel
- MiscellaneousMiscellaneous
- Subpart B—Biological StainsCFR Sub-Part
- Subpart B—Diagnostic DevicesCFR Sub-Part
- Subpart C—Cell And Tissue Culture ProductsCFR Sub-Part
- Subpart C—Clinical Laboratory InstrumentsCFR Sub-Part
- Subpart E—Specimen Preparation ReagentsCFR Sub-Part
- Subpart F—Automated and Semi-Automated Hematology DevicesCFR Sub-Part
- Subpart F—General Hospital and Personal Use Therapeutic DevicesCFR Sub-Part
- Subpart F—Immunological Test SystemsCFR Sub-Part
- Subpart G—Manual Hematology DevicesCFR Sub-Part
- GKGCentrifuge, Hematocrit2Product Code
- GKMHand-Tally, Differential1Product Code
- GJGPipette, Quantitative, Hematology1Product Code
- GJWPipette, Pasteur1Product Code
- GKEOsmotic Fragility Testing1Product Code
- GGGGuaiac Reagent2Product Code
- GGXPipette, Sahli1Product Code
- GGYPipette, Diluting1Product Code
- GHCTube, Sedimentation Rate1Product Code
- GHOHemocytometer1Product Code
- GHYHematocrit, Tube, Rack, Sealer, Holder2Product Code
- GIOTube, Collection, Capillary Blood1Product Code
- K972969QUICK-DRAW CAPILLARY WHOLE BLOOD COLLECTION SYSTEM1Cleared 510(K)
- K941291MONOJECT SAMPLETTE SEPARATOR TUBE1Cleared 510(K)
- K894851TRU-TRAX1Cleared 510(K)
- K885324HEMA(PRO)TEC(TION)1Cleared 510(K)
- K885138CAPILLARY TUBE, BLOOD COLLECTION1Cleared 510(K)
- K884623SAFE-TEC CAPILLARY BLOOD COLLECTION TUBE1Cleared 510(K)
- K881262CARAWAY TUBES, HEPARIN AND PLAIN1Cleared 510(K)
- K881187NATELSON TUBES, HEPARIN AND PLAIN1Cleared 510(K)
- K875061MONOJECT SAMPLETTE AMBER CAPILLARY SERUM SEPARATOR1Cleared 510(K)
- K873647VENTRESCREEN CAPILLARY BLOOD COLLECTION TUBE1Cleared 510(K)
- K850806CORNING BLOOD COLLECTION CAPILLARY TUBES1Cleared 510(K)
- K843608CAPILLARY BLOOD COLLECTION TUBE1Cleared 510(K)
- K843892MICRO HEMATOCRIT CAPILLARY TUBES1Cleared 510(K)
- K843361MINICAPS1Cleared 510(K)
- K843362RINGCAPS1Cleared 510(K)
- K832578MONOJET SAMPLETTE ADAPTERS1Cleared 510(K)
- K812969S/P CAPILLARY TUBES, HEPARINIZED (2A)1Cleared 510(K)
- K812970S/P CAPILLARY TUBES, HEPARINIZED (3A)1Cleared 510(K)
- K812922S/P SURE-CAP C1Cleared 510(K)
- K812923S/P SURE-CAP N1Cleared 510(K)
- K812921S/P SURE-CAP1Cleared 510(K)
- K770981LANCER CAPILLARY BLOOD SERUM SEPARATOR1Cleared 510(K)
- GKWAggregometer, Platelet, Thrombokinetogram2Product Code
- GLGPlatelet Counting, Manual1Product Code
- JBXAggregrometer, Platelet2Product Code
- JBYAggregometer, Platelet, Photo-Optical Scanning2Product Code
- JBZStudy, Platelet Adhesive2Product Code
- JCADevice, Bleeding Time2Product Code
- JIOBlood, Occult, Colorimetric, In Urine2Product Code
- JIPBlood, Occult, Enzymatic Method, In Urine2Product Code
- JPHTest, Erythrocyte Sedimentation Rate1Product Code
- JPIDevice, Hematocrit Measuring2Product Code
- KHEReagent, Occult Blood2Product Code
- OOXAutomated Occult Blood Analyzer2Product Code
- OSLControl, Fecal Occult Blood2Product Code
- Subpart G—Tumor Associated Antigen immunological Test SystemsCFR Sub-Part
- Subpart H—Hematology Kits and PackagesCFR Sub-Part
- Subpart I—Hematology ReagentsCFR Sub-Part
- Subpart J—Products Used In Establishments That Manufacture Blood and Blood ProductsCFR Sub-Part
- Subpart K—Products Used In Establishments That Manufacture Human Cells, Tissues, and Cellular and Tissue-Based Products (HCT/Ps)CFR Sub-Part
- ImmunologyReview Panel
- MicrobiologyReview Panel
- NeurologyReview Panel
- Obstetrical and GynecologicalReview Panel
- OphthalmicReview Panel
- OrthopedicReview Panel
- PathologyReview Panel
- Physical MedicineReview Panel
- RadiologyReview Panel
- General and Plastic SurgeryReview Panel
- ToxicologyReview Panel
- Medical GeneticsReview Panel
- UnknownReview Panel
MICRO HEMATOCRIT CAPILLARY TUBES
- Page Type
- Cleared 510(K)
- FDA Hosted PDF* The FDA doesn't provide PDFs for all submissions.
- 510(k) Number
- K843892
- 510(k) Type
- Traditional
- Applicant
- ABCO DEALERS, INC.
- Country
- United States
- FDA Decision
- Substantially Equivalent
- Decision Date
- 11/13/1984
- Days to Decision
- 41 days