meddevicedb.com FDA Device Reference

SET -502T PH ESOPHAGEAL MICRO SIZE ELECTRODE

K850778 Class I Traditional
Decision Date
1985-06-13
Sponsor / Applicant
Settler Medical Electronics, Inc.

Technical Specification

510(k) Submission ID K850778
Product Code FFT
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.1400
Decision Date 1985-06-13
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SET -502T PH ESOPHAGEAL MICRO SIZE ELECTRODE received FDA 510(k) clearance under submission number K850778, sponsored by Settler Medical Electronics, 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 1985-06-13.

Classification & Regulation

This clearance is catalogued under FDA product code FFT and 21 CFR 876.1400, within the Gastroenterology, Urology review panel as a Class I device.