Anesthesiology
Review Panel
- MiscellaneousMiscellaneous
- Subpart B—Cardiovascular Diagnostic DevicesCFR Sub-Part
- Subpart B—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
- K923781MXR-2000 FLOWMETER1Cleared 510(K)
- K910316OHMEDA - LOW FLOW FLOWMETER1Cleared 510(K)
- K884973FR6000 FLOWMETER1Cleared 510(K)
- K872718SERIES D FLOWMETER1Cleared 510(K)
- K871452CLASSIC (TM) 200 OXYGEN FLOWMETER1Cleared 510(K)
- K862797AIRCO 2000 SERIES FLOWMETERS1Cleared 510(K)
- K854067SELECT FLOWMETER1Cleared 510(K)
- K851288OXYGEN DELIVERY MEASURING DEVICE1Cleared 510(K)
- K850559PRESSURE RELIEF ADAPTOR1Cleared 510(K)
- K850560FLOWMETER, BACKPRESSURE COMPENSATED, THORPE TUBE1Cleared 510(K)
- K834260RECON-2 FLOW CONTROLLER1Cleared 510(K)
- K812419PRESET FLOWMETER1Cleared 510(K)
- K812183TIMETER-PRODUCED PURITAN BENNETT AIR ADP1Cleared 510(K)
- K812128RECON 11Cleared 510(K)
- K802659RESPIRATORY THERAPY FLOWMETER1Cleared 510(K)
- K802311MO8 OXYGEN FLOWMETER1Cleared 510(K)
- K791900M015 OXYGEN & MA15 AIR1Cleared 510(K)
- K791648MODEL 54 FLOWMETER BACK-PRESSURE TUBE1Cleared 510(K)
- K791220FLOWMETER, BACK PRESSURE COMPENSATED,1Cleared 510(K)
- K791017FLOW LIMITER1Cleared 510(K)
- K791069LINDE OXYGEN THERAPY FLOWMETERS, L33-L341Cleared 510(K)
- K781541FLOMETER1Cleared 510(K)
- K760314FLOWMETER, OXYGEN1Cleared 510(K)
- K760102FLOWMETER, P.C., REDESIGNED VERSION1Cleared 510(K)
- CBAMonitor, Air Embolism, Ultrasonic2Product Code
- CCNFlowmeter, Nonback-Pressure Compensated, Bourdon Gauge1Product Code
- ECXCylinder, Compressed Gas, And Valve1Product Code
- 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
- CardiovascularReview Panel
- ChemistryReview Panel
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- General HospitalReview Panel
- HematologyReview Panel
- ImmunologyReview Panel
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- 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
FLOWMETER, P.C., REDESIGNED VERSION
- Page Type
- Cleared 510(K)
- FDA Hosted PDF* The FDA doesn't provide PDFs for all submissions.
- 510(k) Number
- K760102
- 510(k) Type
- Traditional
- Applicant
- OHIO MEDICAL PRODUCTS
- Country
- United States
- FDA Decision
- Substantially Equivalent
- Decision Date
- 7/16/1976
- Days to Decision
- 23 days