meddevicedb.com FDA Device Reference

PORTABLE STANDARD

K934263 Class I Traditional
Decision Date
1993-11-01
Sponsor / Applicant
Cloverleaf Cycle Co.

Technical Specification

510(k) Submission ID K934263
Product Code IOR
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.3850
Decision Date 1993-11-01
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PORTABLE STANDARD received FDA 510(k) clearance under submission number K934263, sponsored by Cloverleaf Cycle Co.. 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 1993-11-01.

Classification & Regulation

This clearance is catalogued under FDA product code IOR and 21 CFR 890.3850, within the Physical Medicine review panel as a Class I device.