meddevicedb.com FDA Device Reference

FINGER MUSCLE TESTER

K770164 Class II Traditional
Decision Date
1977-01-28
Sponsor / Applicant
Bel-Art Products

Technical Specification

510(k) Submission ID K770164
Product Code ISD
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.5360
Decision Date 1977-01-28
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

FINGER MUSCLE TESTER received FDA 510(k) clearance under submission number K770164, sponsored by Bel-Art Products. 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 1977-01-28.

Classification & Regulation

This clearance is catalogued under FDA product code ISD and 21 CFR 890.5360, within the Physical Medicine review panel as a Class II device.