Cleared Traditional

K150037 - Sensus Healthcare Superficial X-ray Rad...

K150037 is an FDA 510(k) clearance for Sensus Healthcare Superficial X-ray Rad..., manufactured by Sensus Healthcare. The device is a Class 2 Radiology device with product code JAD cleared through the Traditional 510(k) pathway after a 280-day FDA review.

K150037 · Sensus Healthcare · Radiology device
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Oct 2015
Decision
280d
Days
Class 2
Risk

K150037 is an FDA 510(k) clearance for the Sensus Healthcare Superficial X-ray Radiation Therapy System with Ultrasonic .... Classified as System, Therapeutic, X-ray (product code JAD), Class II - Special Controls.

Submitted by Sensus Healthcare (Boca Raton, US). The FDA issued a Cleared decision on October 16, 2015 after a review of 280 days - an extended review cycle.

This device falls under the Radiology FDA review panel, regulated under 21 CFR 892.5900 - the FDA radiology and imaging software oversight framework. The Traditional 510(k) pathway establishes clearance through substantial equivalence to a legally marketed predicate device, without requiring clinical trial data.

Device pattern: Standard predicate-based submission. Standard predicate reliance. This clearance follows a standard predicate-based equivalence path within the Radiology review framework, consistent with the majority of Class II 510(k) submissions.

View all Sensus Healthcare devices

FDA 510(k) Submission Details - K150037

510(k) Number K150037 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received January 09, 2015
Decision Date October 16, 2015
Days to Decision 280 days
Submission Type Traditional
Review Panel Radiology (RA)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
173d slower than avg
Panel avg: 107d · This submission: 280d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

JAD Device Classification - Class 2, Special Controls

Product Code JAD System, Therapeutic, X-ray
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 892.5900
What this classification means

Class II devices require demonstration of substantial equivalence to a legally marketed predicate device. This pathway does not require clinical trials - it relies on engineering equivalence and performance data. Most Radiology devices follow this clearance model.

Regulatory Peers - JAD System, Therapeutic, X-ray

All 17
Devices cleared under the same product code (JAD) and FDA review panel - the closest regulatory comparables to K150037.
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