Persyst 15 EEG Review and Analysis Software (Persyst 15 (P15))
K-Number: K242446 · 2025-01-22
Device Summary
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. The listed applicant is Persyst Development Corporation. The 510(k) number is K242446.
When did Persyst 15 EEG Review and Analysis Software (Persyst 15 (P15)) receive FDA 510(k) clearance?
Persyst 15 EEG Review and Analysis Software (Persyst 15 (P15)) received FDA 510(k) clearance on 2025-01-22, under 510(k) number K242446.
Who is the listed applicant for Persyst 15 EEG Review and Analysis Software (Persyst 15 (P15))?
The FDA 510(k) record lists Persyst Development Corporation as the applicant. This does not by itself establish the device manufacturer.
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.
Other records listing Persyst Development Corporation as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: OMB)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.