meddevicedb.com FDA Device Reference

OBTHOSES

K821641 Class I Traditional
Decision Date
1982-06-11
Sponsor / Applicant
Fred Sammons, Inc.

Technical Specification

510(k) Submission ID K821641
Product Code IQI
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.3475
Decision Date 1982-06-11
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

OBTHOSES received FDA 510(k) clearance under submission number K821641, 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 1982-06-11.

Classification & Regulation

This clearance is catalogued under FDA product code IQI and 21 CFR 890.3475, within the Physical Medicine review panel as a Class I device.