meddevicedb.com FDA Device Reference

NON-A-THERM

K792037 Class II Traditional
Decision Date
1979-11-13
Sponsor / Applicant
Labarge, Inc.

Technical Specification

510(k) Submission ID K792037
Product Code KOD
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.5130
Decision Date 1979-11-13
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

NON-A-THERM received FDA 510(k) clearance under submission number K792037, sponsored by Labarge, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Gastroenterology, Urology review panel. The statutory decision date of record is 1979-11-13.

Classification & Regulation

This clearance is catalogued under FDA product code KOD and 21 CFR 876.5130, within the Gastroenterology, Urology review panel as a Class II device.