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BURNETT-KETCHUM DYNAMIC HAND EXERCISER

K790527 Class I Traditional
Decision Date
1979-03-22
Sponsor / Applicant
Maddak, Inc.

Technical Specification

510(k) Submission ID K790527
Product Code JFA
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.5410
Decision Date 1979-03-22
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

BURNETT-KETCHUM DYNAMIC HAND EXERCISER received FDA 510(k) clearance under submission number K790527, sponsored by Maddak, 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 1979-03-22.

Classification & Regulation

This clearance is catalogued under FDA product code JFA and 21 CFR 890.5410, within the Physical Medicine review panel as a Class I device.