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Sensus Healthcare Superficial X-ray Radiation Therapy System with Ultrasonic Imaging Capabilities

K150037 Class II Traditional
Decision Date
2015-10-16
Sponsor / Applicant
Sensus Healthcare

Technical Specification

510(k) Submission ID K150037
Product Code JAD
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.5900
Decision Date 2015-10-16
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Sensus Healthcare Superficial X-ray Radiation Therapy System with Ultrasonic Imaging Capabilities received FDA 510(k) clearance under submission number K150037, sponsored by Sensus Healthcare. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2015-10-16.

Classification & Regulation

This clearance is catalogued under FDA product code JAD and 21 CFR 892.5900, within the Radiology review panel as a Class II device.