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
- 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
Warmer, Blood, Electromagnetic Radiation
- Page Type
- Product Code
- Regulation Medical Specialty
- Hematology
- Review Panel
- Hematology
- Submission Type
- PMA
- Device Classification
- Class 3
- Regulation Number
- 864.9205
- GMP Exempt?
- No
- Summary Malfunction Reporting
- Eligible
- Implanted Device
- No
- Life-Sustain/Support Device
- No
- Third Party Review
- Not Third Party Eligible
- MAUDE Alerts
- View and Sign Up For MAUDE Alerts
CFR § 864.9205 Blood and plasma warming device
§ 864.9205 Blood and plasma warming device.
(a) Nonelectromagnetic blood or plasma warming device—(1) Identification. A nonelectromagnetic blood and plasma warming device is a device that warms blood or plasma, by means other than electromagnetic radiation, prior to administration.
(2) Classification. Class II (performance standards).
(b) Electromagnetic blood and plasma warming device—(1) Identification. An electromagnetic blood and plasma warming device is a device that employs electromagnetic radiation (radiowaves or microwaves) to warm a bag or bottle of blood or plasma prior to administration.
(2) Classfication. Class III (premarket approval).
(c) Date PMA or notice of completion of a PDP is required. No effective date has been established of the requirement for premarket approval for the device described in paragraph (b)(1). See § 864.3.
[45 FR 60642, Sept. 12, 1980, as amended at 52 FR 17733, May 11, 1987]