meddevicedb.com FDA Device Reference

X-RAY TUBE HOUSING ASSEMBLY, VARIOUS MODELS

K894413 Class I Traditional
Decision Date
1989-09-22
Sponsor / Applicant
Inmark Corp.

Technical Specification

510(k) Submission ID K894413
Product Code ITY
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.1760
Decision Date 1989-09-22
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

X-RAY TUBE HOUSING ASSEMBLY, VARIOUS MODELS received FDA 510(k) clearance under submission number K894413, sponsored by Inmark Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 1989-09-22.

Classification & Regulation

This clearance is catalogued under FDA product code ITY and 21 CFR 892.1760, within the Radiology review panel as a Class I device.