Anesthesiology
Review Panel
- Cardiovascular Diagnostic DevicesCFR Sub-Part
- Cardiovascular Monitoring DevicesCFR Sub-Part
- Cardiovascular Therapeutic DevicesCFR Sub-Part
- Diagnostic DevicesCFR Sub-Part
- MiscellaneousCFR Sub-Part
- BRXStool, Anesthesia1Product Code
- BRYCabinet, Table And Tray, Anesthesia1Product Code
- BSYCatheters, Suction, Tracheobronchial1Product Code
- BTICompressor, Air, Portable2Product Code
- BXJClip, Nose1Product Code
- BXKGas, Calibration (Specified Concentration)1Product Code
- BZNCart, Emergency, Cardiopulmonary (Excluding Equipment)1Product Code
- CAMYoke Assembly, Medical Gas1Product Code
- CCXSupport, Patient Position1Product Code
- OFOAirway Suction Kit1Product Code
- OFRTracheobronchial Suction Catheter Kit1Product Code
- OFSTracheal Suction Set1Product Code
- OYINon-Bronchoscopic Bronchoalveolar Lavage Catheter1Product Code
- BSDAnalyzer, Gas, Nitrogen, Partial Pressure, Blood-Phase, Non-Indwelling3Product Code
- LSZVentilator, High Frequency3Product Code
- LYMDevice, Cpr AssistUProduct Code
- MNQStimulator, Hypoglossal Nerve, Implanted, Apnea3Product Code
- NJKValve, Pulmonary3Product Code
- OAZOne-Way Air-Leak ValveFProduct Code
- OIRDiaphragmatic/Phrenic Nerve Laparoscopically-Implanted StimulatorFProduct Code
- OOYBronchial Thermoplasty System3Product Code
- PDRComputer-Assisted Personalized Sedation System3Product Code
- PNCCatheter IntroducerNProduct Code
- POILung Tissue Sealant For Lung Volume ReductionNProduct Code
- PSRImplanted Phrenic Nerve Stimulator For Central Sleep Apnea3Product Code
- QGZElectrical Tumor Treatment Fields3Product Code
- QKSInhaler, Metered Dose Or Dry Powder, Cder Or Cber LedNProduct Code
- QLIVaporizer, Cder Or Cber LedNProduct Code
- QOQNon-Continuous Ventilator For Emergency UseNProduct Code
- QORContinuous Ventilator, Minimal Ventilatory SupportNProduct Code
- QOUEmergency ResuscitatorNProduct Code
- QOWVentilatory Assistance HelmetNProduct Code
- QPRNeurological Stimulation For Emergency UseNProduct Code
- QRSDevice For Sleep Apnea Testing Based On Mandibular Movement2Product Code
- QSFSoftware Option For Anesthesia Gas Machine To Achieve And Maintain Targeted End Tidal Oxygen And Anesthetic Agents3Product Code
- Submissions with No Product CodeMiscellaneous
- Monitoring DevicesCFR Sub-Part
- Neurological Therapeutic DevicesCFR Sub-Part
- Physical Medicine Therapeutic DevicesCFR Sub-Part
- Prosthetic DevicesCFR Sub-Part
- Surgical DevicesCFR Sub-Part
- Therapeutic DevicesCFR Sub-Part
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Tracheal Suction Set
- Page Type
- Product Code
- Definition
- This product code has been established in accordance with the may 20, 1997, guidance entitled, convenience kits interim regulatory guidance, found at www.Fda.Gov/cdrh/ode/convkit.Html. This type of convenience kit, as listed in the guidance above, is under enforcement discretion, and does not require a premarket notification (510(k)) to market if it meets all criteria in the guidance.
- Physical State
- This product code has been established in accordance with the May 20, 1997, Guidance entitled, Convenience Kits Interim Regulatory Guidance, found at www.fda.gov/cdrh/ode/convkit.html. This type of convenience kit, as listed in the guidance above, is under enforcement discretion, and does not require a premarket notification (510(k)) to market if it meets all criteria in the guidance.
- Technical Method
- This product code has been established in accordance with the May 20, 1997, Guidance entitled, Convenience Kits Interim Regulatory Guidance, found at www.fda.gov/cdrh/ode/convkit.html. This type of convenience kit, as listed in the guidance above, is under enforcement discretion, and does not require a premarket notification (510(k)) to market if it meets all criteria in the guidance.
- Target Area
- This product code has been established in accordance with the May 20, 1997, Guidance entitled, Convenience Kits Interim Regulatory Guidance, found at www.fda.gov/cdrh/ode/convkit.html. This type of convenience kit, as listed in the guidance above, is under enforcement discretion, and does not require a premarket notification (510(k)) to market if it meets all criteria in the guidance.
- Regulation Medical Specialty
- Anesthesiology
- Review Panel
- Anesthesiology
- Submission Type
- Enforcement Discretion
- Device Classification
- Class 1
- Regulation Number
- 868.6810
- 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 § 868.6810 Tracheobronchial suction catheter
§ 868.6810 Tracheobronchial suction catheter.
(a) Identification. A tracheobronchial suction catheter is a device used to aspirate liquids or semisolids from a patient's upper airway.
(b) Classification. Class 1 (general controls). The device is exempt from the premarket notification procedures in subpart E of part 807 of this chapter subject to § 868.9.
[47 FR 31142, July 16, 1982, as amended at 65 FR 2314, Jan. 14, 2000]