meddevicedb.com FDA Device Reference

LOWER BODY CYCLES

K935061 Class I Traditional
Decision Date
1994-09-16
Sponsor / Applicant
Biodex Medical Systems, Inc.

Technical Specification

510(k) Submission ID K935061
Product Code BXB
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.5380
Decision Date 1994-09-16
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

LOWER BODY CYCLES received FDA 510(k) clearance under submission number K935061, sponsored by Biodex Medical Systems, 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 1994-09-16.

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.