meddevicedb.com FDA Device Reference

X-RAY FILM, CONVEY OR SYSTEM

K760279 Class II Traditional
Decision Date
1976-08-13
Sponsor / Applicant
Mallinckrodt Group, Inc.

Technical Specification

510(k) Submission ID K760279
Product Code KPX
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.1860
Decision Date 1976-08-13
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

X-RAY FILM, CONVEY OR SYSTEM received FDA 510(k) clearance under submission number K760279, sponsored by Mallinckrodt Group, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 1976-08-13.

Classification & Regulation

This clearance is catalogued under FDA product code KPX and 21 CFR 892.1860, within the Radiology review panel as a Class II device.