Anesthesiology
Review Panel
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- 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
- 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
- BSAWarmer, Blood, Electromagnetic Radiation3Product Code
- BSBWarmer, Blood, Non-Electromagnetic Radiation2Product Code
- GKTSeparator, Automated, Blood Cell, Diagnostic2Product Code
- KSBSet, Transfer (Blood/Plasma)2Product Code
- KSDDevice, Heat-Sealing1Product Code
- KSERefrigerator, Freezer, Blood Storage2Product Code
- KSFKit, Quality Control For Blood Banking Reagents2Product Code
- KSGMedia, Potentiating For In Vitro Diagnostic Use2Product Code
- KSHChamber, Environmental For The Storage Of Platelet Concentrate2Product Code
- KSILectins And Protectins2Product Code
- KSKSolution, Stabilized Enzyme2Product Code
- KSLSolution, Copper Sulfate For Specific Gravity Determinations1Product Code
- KSMSystem, Test, Combs, Automated2Product Code
- KSNCentrifuge, Cell-Washing, Automated For Immuno-Hematology2Product Code
- KSOCentrifuge, Blood-Bank For In Vitro Diagnostic Use1Product Code
- KSPApparatus, Cell-Freezing And Reagents1Product Code
- KSQDevice, Blood Mixing And Blood Weighing1Product Code
- KSRContainer, Empty, For Collection & Processing Of Blood & Blood Components2Product Code
- KSSSupplies, Blood-Bank1Product Code
- KSTSystem, Blood Collection, Vacuum-Assisted, Manual1Product Code
- KSWSystem, Processing For Frozen Blood2Product Code
- KSXSubstance, Blood Grouping Of Non-Human Origin For In Vitro Diagnostic Use2Product Code
- KSYBoxes, View, Blood Grouping1Product Code
- KSZSystem, Test, Automated Blood Grouping And Antibody2Product Code
- KZLDevice, Warming. Blood And Plasma2Product Code
- MMHBlood Establishment Computer Software And Accessories2Product Code
- MYJDevice, Mixing And Weighing, Semi-Automated2Product Code
- MYXSystem, Blood Collection, Vacuum-Assisted, Automated1Product Code
- OQXSelf-Contained Blood Grouping2Product Code
- ORGPlatelet And Plasma Separator For Bone Graft Handling2Product Code
- PBCManual Blood Grouping And Antibody Test Systems2Product Code
- PKGBone Marrow Processing Device To Support Hematopoietic Reconstitution2Product Code
- PMQPeripheral Blood Processing Device For Wound Management2Product Code
- QYCContainer System For The Processing And Storage Of Red Blood Cell Components Under Reduced Oxygen Conditions2Product Code
- Subpart K—Products Used In Establishments That Manufacture Human Cells, Tissues, and Cellular and Tissue-Based Products (HCT/Ps)CFR Sub-Part
- ImmunologyReview Panel
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- UnknownReview Panel
Peripheral Blood Processing Device For Wound Management
- Page Type
- Product Code
- Definition
- Preparation of autologous platelet rich plasma gel from a small sample of peripheral blood for wound management.
- Physical State
- May include centrifuge and sterile single-use tubes and disposables
- Technical Method
- Uses centrifugal methods to separate whole blood into components, after which the platelet rich plasma gel is withdrawn
- Target Area
- Blood drawn from peripheral veins, PRP gel topically applied to exuding cutaneous wounds such as leg ulcers, pressure ulcers and diabetic ulcers, and mechanically or surgically-debrided wounds
- Regulation Medical Specialty
- Hematology
- Review Panel
- Hematology
- Submission Type
- 510(K)
- Device Classification
- Class 2
- Regulation Number
- 864.9245
- GMP Exempt?
- No
- Summary Malfunction Reporting
- Eligible
- Implanted Device
- No
- Life-Sustain/Support Device
- No
- Third Party Review
- Not Third Party Eligible
- MAUDE Alerts
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CFR § 864.9245 Automated blood cell separator
§ 864.9245 Automated blood cell separator.
(a) Identification. An automated blood cell separator is a device that uses a centrifugal or filtration separation principle to automatically withdraw whole blood from a donor, separate the whole blood into blood components, collect one or more of the blood components, and return to the donor the remainder of the whole blood and blood components. The automated blood cell separator device is intended for routine collection of blood and blood components for transfusion or further manufacturing use.
(b) Classification. Class II (special controls). The special control for this device is a guidance for industry and FDA staff entitled “Class II Special Controls Guidance Document: Automated Blood Cell Separator Device Operating by Centrifugal or Filtration Separation Principle.”
[72 FR 67644, Nov. 30, 2007]