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TRAUMA STAND

K852952 Class I Traditional
Decision Date
1985-09-26
Sponsor / Applicant
Xre Corp.

Technical Specification

510(k) Submission ID K852952
Product Code IYB
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.1770
Decision Date 1985-09-26
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

TRAUMA STAND received FDA 510(k) clearance under submission number K852952, sponsored by Xre 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 1985-09-26.

Classification & Regulation

This clearance is catalogued under FDA product code IYB and 21 CFR 892.1770, within the Radiology review panel as a Class I device.