meddevicedb.com FDA Device Reference

MUSCLE TESTING GUN

K791021 Class I Traditional
Decision Date
1979-06-15
Sponsor / Applicant
The Orthodyn Co.

Technical Specification

510(k) Submission ID K791021
Product Code HRW
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.1250
Decision Date 1979-06-15
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MUSCLE TESTING GUN received FDA 510(k) clearance under submission number K791021, sponsored by The Orthodyn Co.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 1979-06-15.

Classification & Regulation

This clearance is catalogued under FDA product code HRW and 21 CFR 888.1250, within the Orthopedic review panel as a Class I device.