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BK-5305 MULTIPLE HAND GRID

K821857 Class I Traditional
Decision Date
1982-07-02
Sponsor / Applicant
Fred Sammons, Inc.

Technical Specification

510(k) Submission ID K821857
Product Code ION
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.5370
Decision Date 1982-07-02
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

BK-5305 MULTIPLE HAND GRID received FDA 510(k) clearance under submission number K821857, 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 1982-07-02.

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.