Anesthesiology
Review Panel
- CardiovascularReview Panel
- ChemistryReview Panel
- DentalReview Panel
- Ear, Nose, ThroatReview Panel
- Gastroenterology and UrologyReview Panel
- MiscellaneousMiscellaneous
- MXQStent, Urethral, External Sphincter, Permanent3Product Code
- NAZStimulator, BladderFProduct Code
- NCVLithotripter, Shockwave (For Treating Gallbladder Stones)3Product Code
- QGGEsophageal Sheath With Distal Balloon Anchor2Product Code
- QJNLaparoscopic Accessories, Esophageal Sizing2Product Code
- QKATemporarily-Placed Urethral Opening System For Symptoms Of Benign Prostatic Hyperplasia2Product Code
- EZZProsthesis, Vas Deferens3Product Code
- FAAReplacer, Urethral3Product Code
- FABReplacer, Ureteral3Product Code
- FACValve, Ureterovesicle3Product Code
- FAGProsthesis, Urethral Sphincter3Product Code
- FAODevice, Cystometric, Air3Product Code
- FBYCooler, Esophageal And Gastric3Product Code
- FBZCooler, Prostatic3Product Code
- LEIImplant, Anti-Gastroesophageal Reflux3Product Code
- LILMonitor, Penile TumescenceUProduct Code
- LJECatheter, NephrostomyUProduct Code
- LKNSeparator, Automated, Blood Cell And Plasma, TherapeuticUProduct Code
- LKXDevice, Thermal, HemorrhoidsUProduct Code
- LNLStimulator, Electrical For Sperm CollectionUProduct Code
- LNMAgent, Bulking, Injectable For Gastro-Urology Use3Product Code
- LNQIntestinal StimulatorFProduct Code
- LNRSystem, Photopheresis, Extracorporeal3Product Code
- LOADevice, Testicular Hypothermia3Product Code
- LQQColumns, Immunoadsorption In Extracorporeal Systems3Product Code
- LQSSpermatocele, AlloplasticUProduct Code
- LRLCushion, HemorrhoidUProduct Code
- LSTDevice, Erectile DysfunctionUProduct Code
- LTIImplant, Intragastric For Morbid Obesity3Product Code
- LXWColumn, Adsorption, Low Density, Lipoprotein3Product Code
- MDPSeparator For Therapeutic Purposes, Membrane Automated Blood Cell/Plasma3Product Code
- MEQSystem, Hyperthermia, Rf/Microwave (Benign Prostatic Hyperplasia),Thermotherapy3Product Code
- MERStent, Urethral, Prostatic, Permanent Or Semi-Permanent3Product Code
- MESStent, Urethral, Bulbous, Permanent Or Semi-Permanent3Product Code
- MIKDevice, Ultrasonic, Thermal Ablation3Product Code
- MIPImplanted Fecal Incontinence Device3Product Code
- MMYLipoprotein, Low Density, Removal3Product Code
- MOAAnalyzer, Diagnostic, Fiber Optic (Colon)3Product Code
- MRESolution, Sodium Hyaluronate3Product Code
- NZCStent, Urethral, Prostatic, Semi-Permanent3Product Code
- OAYLight Source System, Diagnostic Endoscopic3Product Code
- OCKTransurethral Occlusion Insert, Urinary Incontinence-Control, Female3Product Code
- ODHImplantable Bladder-Evacuation Electrical Stimulation SystemFProduct Code
- OKNHyperthermia System, Bladder Cancer Treatment, With Chemotherapy3Product Code
- OVLHemodialyzer, High Cut-OffFProduct Code
- OYFAspiration Therapy System3Product Code
- PATBladder SystemFProduct Code
- PAZElectrical Stimulation Bladder SystemFProduct Code
- PBNApheresis For Focal Glomerulosclerosis In Adult And Pediatric PatientsFProduct Code
- PDIBeta 2-Microglobulin Apheresis ColumnFProduct Code
- PFEGastrointestinal Liner SystemNProduct Code
- PHNProtective Coating, Mucoadhesive Application, For The Rectal MucosaUProduct Code
- PHONormothermic Preservation System For Transplantation Of Initially Unacceptable Donor Lungs3Product Code
- PIKMetabolic Neuromodulation SystemNProduct Code
- PIMNeuromodulator For Obesity3Product Code
- PMHMechanical Compression Device Fecal Incontinence (Non-Manually Operated)FProduct Code
- QBANormothermic Machine Perfusion System For The Preservation Of Standard Criteria Donor Lungs Prior To Transplantation3Product Code
- QLOImmunoadsorption Column For Emergency UseNProduct Code
- QMKExtracorporeal Acoustic Wave Generating Accessory To Urological Indwelling Catheter For Use During Public Health EmergenNProduct Code
- QNBPlasma Processing System For Converting Alpha To Pre-Beta High-Density LipoproteinFProduct Code
- QQKNormothermic Machine Perfusion System For The Preservation Of Donor Livers Prior To Transplantation3Product Code
- QRHCatheter, Balloon, Urethral, Drug-Coated3Product Code
- QPTStimulator, Tibial, Electrical, Implantable, For Urinary Incontinence3Product Code
- QSWEndoscopic Traction Device2Product Code
- QTDEndoscopic Suturing Device For Altering Gastric Anatomy For Weight Loss2Product Code
- QTHEndoscopic Light-Projecting Measuring Device2Product Code
- QTNOrally Ingested Transient Device For Constipation2Product Code
- QUDBlood Detection Capsule2Product Code
- QUNTether Accessory For Use In The Gastrointestinal Tract2Product Code
- QWWNon-Medicated Topical Formulation For Treatment Of Erectile Dysfunction.2Product Code
- QXHGallbladder Drainage Stent And Delivery System2Product Code
- QXMImplanted Tibial Electrical Urinary Continence Device2Product Code
- QEJFlushing Solution For Short Term Storage Of Veins At Room Temperature During Coronary Artery Bypass Graft Surgeries2Product Code
- QXBDrug Coated Prostatic Dilation Catheter For Benign Prostatic Hyperplasia3Product Code
- QZFGastrointestinal Capsule Endoscopy Analysis Software Device2Product Code
- SAKSoftware Device To Aid In The Prediction Or Diagnosis Of Sepsis2Product Code
- SCBDeflation Needle For Removal Of Intragastric Balloon2Product Code
- QNAUltrasonic Urinary Stone Propulsion Device2Product Code
- SDQAlfapump System3Product Code
- Submissions with No Product CodeMiscellaneous
- Subpart B—Diagnostic DevicesCFR Sub-Part
- Subpart B—Obstetrical and Gynecological Diagnostic DevicesCFR Sub-Part
- Subpart C—Cardiovascular Monitoring DevicesCFR Sub-Part
- Subpart C—Monitoring DevicesCFR Sub-Part
- Subpart D—Prosthetic DevicesCFR Sub-Part
- Subpart E—Obstetrical and Gynecological Surgical DevicesCFR Sub-Part
- Subpart E—Surgical DevicesCFR Sub-Part
- Subpart F—Neurological Therapeutic DevicesCFR Sub-Part
- Subpart F—Physical Medicine Therapeutic DevicesCFR Sub-Part
- Subpart F—Therapeutic DevicesCFR Sub-Part
- Subpart G—General Hospital and Personal Use Miscellaneous DevicesCFR Sub-Part
- General HospitalReview Panel
- HematologyReview Panel
- 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
Apheresis For Focal Glomerulosclerosis In Adult And Pediatric Patients
- Page Type
- Product Code
- Definition
- Removal of plasma components to treat focal glomerulosclerosis
- Physical State
- Composed of four components: a pair of paheresis columns (dextran sulfate cellulose adsorption column soaked in sodium citrate solution); two other disposable components (a hollow fiber, ethylene vinyl alcohol copolymer-coated polyethylene plasma separator and a polyvinyl chloride tubing system); and a reusable electronic control unit.
- Technical Method
- Blood is pumped from patients arm into the device which then separates blood into cellular components and plasma. Plasma is then sent thru dextran sulfate cellulose column to remove specific plasma components. Depleted plasma is then recombined with cellular blood elements and is then pumped back to patient.
- Target Area
- Plasma components are removed to aid the patients kidneys
- Review Panel
- Gastroenterology and Urology
- Submission Type
- HDE - Humanitarian Device Exemption
- Device Classification
- F
- GMP Exempt?
- No
- Summary Malfunction Reporting
- Ineligible
- Implanted Device
- No
- Life-Sustain/Support Device
- No
- Third Party Review
- Not Third Party Eligible
- MAUDE Alerts
- View and Sign Up For MAUDE Alerts
No Linked CFR Text
The FDA has not linked product code PBN to any particular section of the CFR (Code of Federal Regulations). There are multiple reasons why this might be the case:
- The product code was created for a class III submission that does not follow the normal PMN or PMA path - e.g., for a device that falls under HDE (Humanitarian Device Exemption) or EUA (Emergency Use Authorization).
- The FDA has generated the product code for an existing Class III device, as a result of a PMA supplement that modifies the device in a way that it can't fit under the existing product code originally assigned
- The product code was created for internal use at the FDA, and not for classification or regulatory-related purposes.