ANSiStim-PP— 510(k) K220397

Substantially Equivalent

Dyansys, Inc.

FDA 510(k) clearance K220397 for ANSiStim-PP, Substantially Equivalent on 2022-05-12. Applicant: Dyansys, Inc.. Device class: 2.

Clearance details

Applicant: Dyansys, Inc.
Product code: Code NHI
Device class: Class 2
Regulation: 21 CFR 882.5890
Advisory panel: Neurology
Date received: 2022-02-11
Decision date: 2022-05-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: San Mateo, CA, US

Download summary PDF View on FDA.gov ↗

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