Cleared Traditional

K993530 - SYSTEM 2100

K993530 is an FDA 510(k) clearance for SYSTEM 2100, manufactured by Math Solutions, LLC. The device is a Class 2 Radiology device with product code LLZ cleared through the Traditional 510(k) pathway after a 58-day FDA review.

K993530 · Math Solutions, LLC · Radiology device
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Dec 1999
Decision
58d
Days
Class 2
Risk

K993530 is an FDA 510(k) clearance for the SYSTEM 2100. 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 Math Solutions, LLC (Columbia, US). The FDA issued a Cleared decision on December 15, 1999 after a review of 58 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 Math Solutions, LLC devices

FDA 510(k) Submission Details - K993530

510(k) Number K993530 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received October 18, 1999
Decision Date December 15, 1999
Days to Decision 58 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
49d faster than avg
Panel avg: 107d · This submission: 58d
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 1458
Devices cleared under the same product code (LLZ) and FDA review panel - the closest regulatory comparables to K993530.
INTEGRATED DIGITAL MEDICAL RECORD (IDMR)
K993338 · Ibm Israel , Ltd. · Dec 1999
CARDIOVASCULAR MEASUREMENT SYSTEM - VIEW
K993761 · Medis Medical Imaging Systems BV · Dec 1999
PHILIPS INTURIS DICOM RECORDER
K993227 · Philips Medical Systems North America, Inc. · Dec 1999
DDS, DS3000, RS3000, CS5000, OT3000, IS3000, RS5000, CD3000, US3000, (AMONGST OTHER NAMES)
K993532 · Impax Technology, Inc. · Dec 1999
AX WORKSTATION DR-VIEWER SOFTWARE OPTION
K992925 · Siemens Corp. · Nov 1999
POWERVIEW ULTRASOUND WORKSTATION, UIDM-400A
K992886 · Toshiba America Medical Systems, In.C · Nov 1999