Cleared Abbreviated

K141329 - RADSPA

K141329 is an FDA 510(k) clearance for RADSPA, manufactured by Telerad Tech Private Limited. The device is a Class 2 Radiology device with product code LLZ cleared through the Abbreviated 510(k) pathway after a 30-day FDA review.

K141329 · Telerad Tech Private Limited · Radiology device
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Jun 2014
Decision
30d
Days
Class 2
Risk

K141329 is an FDA 510(k) clearance for the RADSPA. Classified as System, Image Processing, Radiological within the LLZ classification (a category encompassing advanced image processing and PACS-adjacent software), Class II - Special Controls.

Submitted by Telerad Tech Private Limited (Aurora, US). The FDA issued a Cleared decision on June 20, 2014 after a review of 30 days - a notably fast clearance cycle.

This device falls under the Radiology FDA review panel, regulated under 21 CFR 892.2050 - the FDA radiology and imaging software oversight framework. The Abbreviated 510(k) pathway was used, relying on FDA-recognized standards to demonstrate substantial equivalence.

Device pattern: Incremental AI imaging tool. Standards-verified equivalence. Overall, this clearance reflects a predicate-aligned approval typical of modern AI radiology extensions - not a novel clinical breakthrough, but a validated iteration within an established regulatory category.

View all Telerad Tech Private Limited devices

FDA 510(k) Submission Details - K141329

510(k) Number K141329 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received May 21, 2014
Decision Date June 20, 2014
Days to Decision 30 days
Submission Type Abbreviated
Review Panel Radiology (RA)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
77d faster than avg
Panel avg: 107d · This submission: 30d
Pathway characteristics
Standards-based clearance path.

LLZ Device Classification - Class 2, Special Controls

Product Code LLZ System, Image Processing, Radiological
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 892.2050
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 - LLZ System, Image Processing, Radiological

All 1236
Devices cleared under the same product code (LLZ) and FDA review panel - the closest regulatory comparables to K141329.
SYNGO.MR NEUROLOGY, SYNGO.MMR GENERAL
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ESIE APPS SUITE
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QUENTRY DOSE REVIEW
K141199 · Brainlab AG · Jun 2014
PLANMECA ROMEXIS
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PICTURE ARCHIVING AND COMMUNICATIONS SYSTEM
K140960 · Hologic, Inc. · Jun 2014
VITREA IMAGE DENOISING SOFTWARE
K140395 · Vital Images, Inc. · May 2014