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TOENNIES NEUROSCREEN SYSTEM

K972419 Class II Traditional
Decision Date
1998-04-30
Sponsor / Applicant
Erich Jaeger, Inc.

Technical Specification

510(k) Submission ID K972419
Product Code IKN
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.1375
Decision Date 1998-04-30
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

TOENNIES NEUROSCREEN SYSTEM received FDA 510(k) clearance under submission number K972419, sponsored by Erich Jaeger, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Physical Medicine review panel. The statutory decision date of record is 1998-04-30.

Classification & Regulation

This clearance is catalogued under FDA product code IKN and 21 CFR 890.1375, within the Physical Medicine review panel as a Class II device.