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INFRARED EXPOSURE HAND SWITCH

K930049 Class II Traditional
Decision Date
1993-06-22
Sponsor / Applicant
Mid X-Ray, Inc.

Technical Specification

510(k) Submission ID K930049
Product Code IZL
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.1720
Decision Date 1993-06-22
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

INFRARED EXPOSURE HAND SWITCH received FDA 510(k) clearance under submission number K930049, sponsored by Mid X-Ray, 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 1993-06-22.

Classification & Regulation

This clearance is catalogued under FDA product code IZL and 21 CFR 892.1720, within the Radiology review panel as a Class II device.