meddevicedb.com FDA Device Reference

ELEMENT, WORKING

K760184 Class II Traditional
Decision Date
1976-12-02
Sponsor / Applicant
V. Mueller O.V. Baxter Healthcare Corp.

Technical Specification

510(k) Submission ID K760184
Product Code FDC
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.1500
Decision Date 1976-12-02
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ELEMENT, WORKING received FDA 510(k) clearance under submission number K760184, sponsored by V. Mueller O.V. Baxter Healthcare Corp.. 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 1976-12-02.

Classification & Regulation

This clearance is catalogued under FDA product code FDC and 21 CFR 876.1500, within the Gastroenterology, Urology review panel as a Class II device.