Cleared Traditional

K844714 - SELECTRON LDR SELECTRON LOW DOSE RATE

K844714 is an FDA 510(k) clearance for SELECTRON LDR SELECTRON LOW DOSE RATE, manufactured by Radiochemical Co.. The device is a Class 2 Radiology device with product code JAQ cleared through the Traditional 510(k) pathway after a 85-day FDA review.

K844714 · Radiochemical Co. · Radiology device
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Feb 1985
Decision
85d
Days
Class 2
Risk

K844714 is an FDA 510(k) clearance for the SELECTRON LDR SELECTRON LOW DOSE RATE. Classified as System, Applicator, Radionuclide, Remote-controlled (product code JAQ), Class II - Special Controls.

Submitted by Radiochemical Co. (Kanata Ontario Canada, CA). The FDA issued a Cleared decision on February 26, 1985 after a review of 85 days - a notably fast clearance cycle.

This device falls under the Radiology FDA review panel, regulated under 21 CFR 892.5700 - 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 Radiochemical Co. devices

FDA 510(k) Submission Details - K844714

510(k) Number K844714 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received December 03, 1984
Decision Date February 26, 1985
Days to Decision 85 days
Submission Type Traditional
Review Panel Radiology (RA)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
22d faster than avg
Panel avg: 107d · This submission: 85d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

JAQ Device Classification - Class 2, Special Controls

Product Code JAQ System, Applicator, Radionuclide, Remote-controlled
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 892.5700
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 - JAQ System, Applicator, Radionuclide, Remote-controlled

All 182
Devices cleared under the same product code (JAQ) and FDA review panel - the closest regulatory comparables to K844714.
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