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PATIENT GUIDED ELBOW & SHOULDER EXERC

K830793 Class I Traditional
Decision Date
1983-06-16
Sponsor / Applicant
Richard'S Medical Equip., Inc.

Technical Specification

510(k) Submission ID K830793
Product Code BXB
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.5380
Decision Date 1983-06-16
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PATIENT GUIDED ELBOW & SHOULDER EXERC received FDA 510(k) clearance under submission number K830793, sponsored by Richard'S Medical Equip., 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 1983-06-16.

Classification & Regulation

This clearance is catalogued under FDA product code BXB and 21 CFR 890.5380, within the Physical Medicine review panel as a Class I device.