Cleared Traditional

K000052 - X-RAY MONOBLOCK, MONOBLOCK XRS-60-330

K000052 is an FDA 510(k) clearance for X-RAY MONOBLOCK, manufactured by Dynarad Corp.. The device is a Class 1 Radiology device with product code ITY cleared through the Traditional 510(k) pathway after a 34-day FDA review.

K000052 · Dynarad Corp. · Radiology device
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Feb 2000
Decision
34d
Days
Class 1
Risk

K000052 is an FDA 510(k) clearance for the X-RAY MONOBLOCK, MONOBLOCK XRS-60-330. Classified as Assembly, Tube Housing, X-ray, Diagnostic (product code ITY), Class I - General Controls.

Submitted by Dynarad Corp. (Deer Park, US). The FDA issued a Cleared decision on February 10, 2000 after a review of 34 days - a notably fast clearance cycle.

This device falls under the Radiology FDA review panel, regulated under 21 CFR 892.1760 - 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: Fast-track predicate clearance. Standard predicate reliance. The short review cycle indicates strong predicate alignment - the FDA found sufficient equivalence without extended technical review.

View all Dynarad Corp. devices

FDA 510(k) Submission Details - K000052

510(k) Number K000052 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received January 07, 2000
Decision Date February 10, 2000
Days to Decision 34 days
Submission Type Traditional
Review Panel Radiology (RA)
Summary Statement
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
73d faster than avg
Panel avg: 107d · This submission: 34d
Pathway characteristics
Predicate-based equivalence.

ITY Device Classification - Class 1, General Controls

Product Code ITY Assembly, Tube Housing, X-ray, Diagnostic
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 892.1760
What this classification means

Class I devices are subject to general controls only and most are exempt from 510(k) premarket notification. They represent the lowest regulatory burden in the FDA device framework.

Regulatory Peers - ITY Assembly, Tube Housing, X-ray, Diagnostic

All 12
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