Neurotronics

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Web: http://www.neurotronics.com
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Address: 912 NE 2nd Street, Suite 5, Gainesville, Florida 32601, USA
Phone: +1-(352)-372-9955 | Fax: +1-(815)-550-2871 | Map/Directions >>

Profile: Neurotronics develops sleep analysis devices and software. Our product line includes PolySmith™, SurveySmith™, PolySmith™DMS, template builder, tracer, sphinx USB sleep amplifier & echo. Our PolySmith™ DMS is a centralized database with patient scheduling, basic searching & advanced queries. The sphinx offers 33 physiological inputs, integrated pressure transducer & pulse oximeter. The echo device connects to any PSG or EEG amplifier to generate calibration signals on inputs or playback recorded as physiological data.

The company has revenues of < USD 1 Million.

FDA Registration Number: 1063925

9 Products/Services (Click for related suppliers)

• Electroencephalograph Test Signal Generator (FDA Code: GWR / 882.1430)

An electroencephalograph test signal generator is a device used to test or calibrate an electroencephalograph.

• Electroencephalographs (FDA Code: GWQ / 882.1400)

An electroencephalograph is a device used to measure and record the electrical activity of the patient's brain obtained by placing two or more electrodes on the head.

• Medical Software Solutions

• Oximeters (FDA Code: DQA / 870.2700)

An oximeter is a device used to transmit radiation at a known wavelength(s) through blood and to measure the blood oxygen saturation based on the amount of reflected or scattered radiation. It may be used alone or in conjunction with a fiberoptic oximeter catheter.

• Physiological Signal Amplifier (FDA Code: GWL / 882.1835)

A physiological signal amplifier is a general purpose device used to electrically amplify signals derived from various physiological sources (e.g., the electroencephalogram).

• Sleep Diagnostic Software

• Sleep Disorder Treatment Facilities

• Sleep-patient Management Software

• Ventilatory Effort Recorder (FDA Code: MNR / 868.2375)

A breathing (ventilatory) frequency monitor is a device intended to measure or monitor a patient's respiratory rate. The device may provide an audible or visible alarm when the respiratory rate, averaged over time, is outside operator settable alarm limits. This device does not include the apnea monitor classified in 868.2377.