meddevicedb.com FDA Device Reference

ESCORT

K820858 Class I Traditional
Decision Date
1982-04-08
Sponsor / Applicant
Amigo Sales, Inc.

Technical Specification

510(k) Submission ID K820858
Product Code INM
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.3100
Decision Date 1982-04-08
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ESCORT received FDA 510(k) clearance under submission number K820858, sponsored by Amigo Sales, 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 1982-04-08.

Classification & Regulation

This clearance is catalogued under FDA product code INM and 21 CFR 890.3100, within the Physical Medicine review panel as a Class I device.