Anesthesiology
Review Panel
- MiscellaneousMiscellaneous
- Subpart B—Cardiovascular Diagnostic DevicesCFR Sub-Part
- Subpart B—Diagnostic DevicesCFR Sub-Part
- Subpart B—Neurological Diagnostic DevicesCFR Sub-Part
- Subpart C—Cardiovascular Monitoring DevicesCFR Sub-Part
- Subpart C—Monitoring DevicesCFR Sub-Part
- BXHGauge, Gas Pressure, Cylinder/Pipeline1Product Code
- BXMStimulator, Nerve, Ac-Powered2Product Code
- BXNStimulator, Nerve, Battery-Powered2Product Code
- BXOTransducer, Gas Pressure1Product Code
- BXPTransducer, Gas Flow1Product Code
- BXXCalibrator, Pressure, Gas1Product Code
- BXYFlowmeter, Calibration, Gas1Product Code
- BYMTube, Thorpe, Uncompensated1Product Code
- BYRTransducer, Gas Pressure, Differential1Product Code
- BZQMonitor, Breathing Frequency2Product Code
- CANRegulator, Pressure, Gas Cylinder1Product Code
- CAPMonitor, Airway Pressure (Includes Gauge And/Or Alarm)2Product Code
- CAXFlowmeter, Tube, Thorpe, Back-Pressure Compensated1Product Code
- CBAMonitor, Air Embolism, Ultrasonic2Product Code
- CCNFlowmeter, Nonback-Pressure Compensated, Bourdon Gauge1Product Code
- ECXCylinder, Compressed Gas, And Valve1Product Code
- K161179Intelli-Ox1Cleared 510(K)
- K161472Walk-O2-Bout1Cleared 510(K)
- K153518Medipure Oxygen-LC System1Cleared 510(K)
- K143060Intelli-Ox1Cleared 510(K)
- K142149OXYTOTE INFINITY SERIES VIPR SYSTEMS1Cleared 510(K)
- K132778GRAB 'N GO PLUS, GRAB 'N GO DIGITAL1Cleared 510(K)
- K131386EZ-OX PLUS GENERATION II1Cleared 510(K)
- K101792LIV LINDE INTERGRATED VALVE-PORTABLE OXYGEN SYSTEM, MODEL M7061Cleared 510(K)
- K063354LINDE INTEGRATED VALVE (LIV)1Cleared 510(K)
- K062300OX-SOX, MODEL C, D, E,1Cleared 510(K)
- K053117EZ-OX PLUS1Cleared 510(K)
- K033897MEDICYL-E-LITE PORTABLE OXYGEN DELIVERY SYSTEM1Cleared 510(K)
- K771246ALARM SYS FOR NITROUS OXIDE SYS.1Cleared 510(K)
- FLSMonitor, Apnea, Facility Use2Product Code
- JAXPneumotachometer2Product Code
- JEZMonitor, Lung Water Measurement3Product Code
- KLKMonitor, Oxygen, Cutaneous, For Infant Not Under Gas Anesthesia2Product Code
- KOIStimulator, Nerve, Peripheral, Electric2Product Code
- LKDMonitor, Carbon-Dioxide, Cutaneous2Product Code
- LPPMonitor, Oxygen, Cutaneous, For Uses Other Than For Infant Not Under Gas Anesthesia2Product Code
- MNRVentilatory Effort Recorder2Product Code
- MRPAnalyzer, Nitric Oxide2Product Code
- MRQAnalyzer, Nitrogen Dioxide2Product Code
- NPFMonitor, Apnea, Home Use2Product Code
- PRKDevice Indicating An Exhalation Event2Product Code
- PUGAnalyzer, Nitrogen Dioxide, Exempt2Product Code
- PXEPressure Monitoring (Air/Gas) Kit1Product Code
- Subpart D—Prosthetic DevicesCFR Sub-Part
- Subpart E—Surgical DevicesCFR Sub-Part
- Subpart F—Cardiovascular Therapeutic 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—MiscellaneousCFR Sub-Part
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ALARM SYS FOR NITROUS OXIDE SYS.
- Page Type
- Cleared 510(K)
- 510(k) Number
- K771246
- 510(k) Type
- Traditional
- Applicant
- STAR DENTAL MFG. CO.
- Country
- United States
- FDA Decision
- Substantially Equivalent
- Decision Date
- 7/15/1977
- Days to Decision
- 4 days