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BIOFEEDBACK SYSTEM FOR SPEECH DISORDERS

K942651 Class I Traditional
Decision Date
1995-10-19
Sponsor / Applicant
Casa Futura Technologies

Technical Specification

510(k) Submission ID K942651
Product Code KTH
Medical Specialty / Panel Ear, Nose, Throat
Regulation Citation 21 CFR 874.5840
Decision Date 1995-10-19
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

BIOFEEDBACK SYSTEM FOR SPEECH DISORDERS received FDA 510(k) clearance under submission number K942651, sponsored by Casa Futura Technologies. The device was reviewed via the Traditional premarket notification pathway and assigned to the Ear, Nose, Throat review panel. The statutory decision date of record is 1995-10-19.

Classification & Regulation

This clearance is catalogued under FDA product code KTH and 21 CFR 874.5840, within the Ear, Nose, Throat review panel as a Class I device.