510(k) K213882

Clearance Details

Decision

SESE (Substantially Equivalent)

Decision Date

June 8, 2022

Date Received

December 13, 2021

Clearance Type

Traditional

Expedited Review

No

Third Party Review

No

Device Classification

Device Name

Pediatric Autism Spectrum Disorder Diagnosis Aid

Device Class

Class II

Regulation Number

882.1491

Review Panel

NE

Submission Type

A pediatric Autism Spectrum Disorder diagnosis aid is a prescription device that is intended for use as an aid in the diagnosis of Autism Spectrum Disorder in pediatric patients.