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FINGER EXERCISE BOARD

K772404 Class I Traditional
Decision Date
1978-02-13
Sponsor / Applicant
Fred Sammons, Inc.

Technical Specification

510(k) Submission ID K772404
Product Code ION
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.5370
Decision Date 1978-02-13
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

FINGER EXERCISE BOARD received FDA 510(k) clearance under submission number K772404, sponsored by Fred Sammons, 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 1978-02-13.

Classification & Regulation

This clearance is catalogued under FDA product code ION and 21 CFR 890.5370, within the Physical Medicine review panel as a Class I device.