FDA-Authorized AI Device

Persyst 15 EEG Review and Analysis

Persyst

Persyst 15 adds seizure and spike detection, quantitative trends, artifact reduction, monitoring, and review tools to compatible clinical EEG systems.

At A Glance

Manufacturer
Persyst
Medical specialty
Neurology
Clearance route
510(k)
Year authorized
Multiple clearances
Modality
EEG
Role in workflow
Clinical decision support

Persyst 15 helps clinicians review and monitor full clinical EEG recordings. It does not acquire a rapid bedside study. It works with compatible EEG systems and adds computer-assisted analysis to the recording those systems produce.

What The Software Adds

  • Seizure detection
  • Spike detection and review
  • Quantitative EEG trends
  • Artifact reduction
  • Multi-patient monitoring and remote review

The practical value is review at scale. Continuous EEG can produce hours or days of data. Detection and trend tools help the clinical team find periods that need closer review without turning the software output into the final interpretation.

Where It Fits

Persyst says its software integrates with major EEG manufacturers. That makes compatibility, licensing, review stations, remote access, and the hospital's existing EEG workflow part of the buying decision.

See the manufacturer's current Persyst 15 product and feature information. Compare it with Ceribell Clarity when the question is rapid point-of-care EEG rather than analysis of a conventional recording.

Where It Is Used

  • Continuous EEG monitoring in intensive care
  • Epilepsy monitoring unit review
  • Quantitative EEG trending across long recordings

Limitations Worth Knowing

Detection, trends, and artifact reduction support clinical review. They do not replace review by a qualified clinician, and the value of each output depends on recording quality, electrode coverage, patient context, and the configured workflow.

Confirm the current intended use, compatible EEG systems, licensing, system requirements, and instructions for use before clinical or purchasing decisions.

The FDA's AI-Enabled Medical Device List links to public authorization records.

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