meddevicedb.com FDA Device Reference

BENNETT OVERHEAD TUBE CRANE MODEL NO. B-OTC

K925716 Class I Traditional
Decision Date
1992-12-17
Sponsor / Applicant
Bennett X-Ray Corp.

Technical Specification

510(k) Submission ID K925716
Product Code IYB
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.1770
Decision Date 1992-12-17
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

BENNETT OVERHEAD TUBE CRANE MODEL NO. B-OTC received FDA 510(k) clearance under submission number K925716, sponsored by Bennett X-Ray 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 1992-12-17.

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.