Cleared Traditional

K052460 - POWERSERVER, POWERREADER, GATEWAY AND POWERCACHE

K052460 is an FDA 510(k) clearance for POWERSERVER, manufactured by Ramsoft, Inc.. The device is a Class 2 Radiology device with product code LLZ cleared through the Traditional 510(k) pathway after a 14-day FDA review.

K052460 · Ramsoft, Inc. · Radiology device
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Sep 2005
Decision
14d
Days
Class 2
Risk

K052460 is an FDA 510(k) clearance for the POWERSERVER, POWERREADER, GATEWAY AND POWERCACHE. 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 Ramsoft, Inc. (Toronto, CA). The FDA issued a Cleared decision on September 21, 2005 after a review of 14 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 Traditional 510(k) pathway establishes clearance through substantial equivalence to a legally marketed predicate device, without requiring clinical trial data.

Device pattern: Incremental AI imaging tool. Moderate equivalence dependency. 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 Ramsoft, Inc. devices

FDA 510(k) Submission Details - K052460

510(k) Number K052460 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received September 07, 2005
Decision Date September 21, 2005
Days to Decision 14 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
93d faster than avg
Panel avg: 107d · This submission: 14d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

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 2129
Devices cleared under the same product code (LLZ) and FDA review panel - the closest regulatory comparables to K052460.
SYNGO IMAGING VERSION V20A
K052461 · Siemens AG Medical Solutions · Sep 2005
NIO 2MP-20 AND E-2620 S
K052276 · Barcoview · Sep 2005
HIPAX MEDICAL IMAGING SOFTWARE
K052411 · Steinhart Medizinsysteme GmbH · Sep 2005
CORONIS 2MP-21 AND MFGD 2621
K052403 · Barcoview · Sep 2005
CORONIS 3MP-21 AND MFGD 3621
K052429 · Barcoview · Sep 2005
COLOR LCD MONITOR, MODEL RADIOFORCE R31 & R31-C
K052344 · Eizo Nanao Corporation · Sep 2005