meddevicedb.com FDA Device Reference

DMG100 AND 500 ISOMETRIC STRENGTH DYNAMOMETER

K923262 Class II Traditional
Decision Date
1992-10-27
Sponsor / Applicant
John Chatillon & Sons, Inc.

Technical Specification

510(k) Submission ID K923262
Product Code LBB
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.1240
Decision Date 1992-10-27
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

DMG100 AND 500 ISOMETRIC STRENGTH DYNAMOMETER received FDA 510(k) clearance under submission number K923262, sponsored by John Chatillon & Sons, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 1992-10-27.

Classification & Regulation

This clearance is catalogued under FDA product code LBB and 21 CFR 888.1240, within the Orthopedic review panel as a Class II device.