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FDA 510(k)

Persyst 15 EEG Review and Analysis Software (Persyst 15 (P15))

K-Number: K242446 · 2025-01-22

Decision Date2025-01-22
Product CodeOMB
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

Persyst 15 EEG Review and Analysis Software (Persyst 15 (P15)) is a medical device manufactured by Persyst Development Corporation. It received FDA 510(k) clearance on 2025-01-22 under approval number K242446. The device is classified under product code OMB. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Persyst 15 EEG Review and Analysis Software (Persyst 15 (P15))?

Persyst 15 EEG Review and Analysis Software (Persyst 15 (P15)) is a medical device that received FDA 510(k) clearance on 2025-01-22. It is manufactured by Persyst Development Corporation. The 510(k) number is K242446.

When was Persyst 15 EEG Review and Analysis Software (Persyst 15 (P15)) approved by the FDA?

Persyst 15 EEG Review and Analysis Software (Persyst 15 (P15)) received FDA 510(k) clearance on 2025-01-22, under approval number K242446.

What company makes Persyst 15 EEG Review and Analysis Software (Persyst 15 (P15))?

Persyst 15 EEG Review and Analysis Software (Persyst 15 (P15)) is manufactured by Persyst Development Corporation.

What is the FDA product code for Persyst 15 EEG Review and Analysis Software (Persyst 15 (P15))?

The FDA product code for Persyst 15 EEG Review and Analysis Software (Persyst 15 (P15)) is OMB.

Related Clinical Trials

Related PubMed Literature

Other Devices by Persyst Development Corporation

Related Devices (Code: OMB)

Official Source

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