meddevicedb.com FDA Device Reference

CANE/REACHER

K780085 Class I Traditional
Decision Date
1978-01-30
Sponsor / Applicant
Fred Sammons, Inc.

Technical Specification

510(k) Submission ID K780085
Product Code IPS
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.3075
Decision Date 1978-01-30
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CANE/REACHER received FDA 510(k) clearance under submission number K780085, sponsored by Fred Sammons, 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 1978-01-30.

Classification & Regulation

This clearance is catalogued under FDA product code IPS and 21 CFR 890.3075, within the Physical Medicine review panel as a Class I device.