Cleared Traditional

K182138 - Precise Treatment System

Also marketed or referenced as:
Synergy platform Synergy Infinity VersaHD

K182138 is the FDA 510(k) clearance for Precise Treatment System by Eleckta Limited. It is a Class 2 Radiology device (product code IYE) cleared through the Traditional 510(k) pathway after a 29-day FDA review.

K182138 · Eleckta Limited · Radiology device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Sep 2018
Decision
29d
Days
Class 2
Risk

K182138 is an FDA 510(k) clearance for the Precise Treatment System. Classified as Accelerator, Linear, Medical (product code IYE), Class II - Special Controls.

Submitted by Eleckta Limited (Crawley, GB). The FDA issued a Cleared decision on September 5, 2018 after a review of 29 days - a notably fast clearance cycle.

This device falls under the Radiology FDA review panel, regulated under 21 CFR 892.5050 - 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 Eleckta Limited devices

Submission Details

510(k) Number K182138 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received August 07, 2018
Decision Date September 05, 2018
Days to Decision 29 days
Submission Type Traditional
Review Panel Radiology (RA)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
78d faster than avg
Panel avg: 107d · This submission: 29d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code IYE Accelerator, Linear, Medical
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 892.5050
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 - IYE Accelerator, Linear, Medical

All 312
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