Cleared Traditional

K093982 - XELERIS 3 PROCESSING AND REVIEW WORKSTATION

K093982 is an FDA 510(k) clearance for XELERIS 3 PROCESSING AND REVIEW WORKSTATION, manufactured by Ge Medical Systems F.I. Haifa. The device is a Class 2 Radiology device with product code LLZ cleared through the Traditional 510(k) pathway after a 15-day FDA review.

K093982 · Ge Medical Systems F.I. Haifa · Radiology device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Jan 2010
Decision
15d
Days
Class 2
Risk

K093982 is an FDA 510(k) clearance for the XELERIS 3 PROCESSING AND REVIEW WORKSTATION. 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 Ge Medical Systems F.I. Haifa (Tirat Hacarmel, IL). The FDA issued a Cleared decision on January 8, 2010 after a review of 15 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 Ge Medical Systems F.I. Haifa devices

FDA 510(k) Submission Details - K093982

510(k) Number K093982 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received December 24, 2009
Decision Date January 08, 2010
Days to Decision 15 days
Submission Type Traditional
Review Panel Radiology (RA)
Summary Summary PDF
Third-party Review Yes - reviewed by an FDA-accredited third party
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
92d faster than avg
Panel avg: 107d · This submission: 15d
Pathway characteristics
Predicate-based equivalence. No clinical trials required. Third-party reviewed.

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 Consultant

Underwriters Laboratories, Inc.
CASEY CONRY

The regulatory consultant manages the 510(k) submission process on behalf of the applicant - coordinating technical documentation, predicate strategy and FDA communications. Identifying the consultant behind a submission is a key signal for competitive regulatory intelligence.

Regulatory Peers - LLZ System, Image Processing, Radiological

All 2147
Devices cleared under the same product code (LLZ) and FDA review panel - the closest regulatory comparables to K093982.
EXAPACS
K093444 · Medincom Technology Corp · Feb 2010
3DI
K093703 · Shina Systems , Ltd. · Jan 2010
PCR ELEVA 1.2
K093355 · Philips Medical Systems, Inc. · Jan 2010
GALILEOS IMPLANT, VERSION 1.7
K093090 · Sicat GmbH & Co. KG · Dec 2009
DICOMPACS, MODEL 5.2, DICOMPACS DX-R, MODEL 1.4
K091364 · Oehm Und Rehbein GmbH · Dec 2009
DIGITAL LIGHTBOX
K093117 · Brainlab AG · Dec 2009