Cleared Traditional

K002782 - HERMES HD AQ ACQUISITION STATION AND HERMES WORKSTATION

K002782 is an FDA 510(k) clearance for HERMES HD AQ ACQUISITION STATION AND HE..., manufactured by Nuclear Diagnostics AB. The device is a Class 2 Radiology device with product code LLZ cleared through the Traditional 510(k) pathway after a 90-day FDA review.

K002782 · Nuclear Diagnostics AB · Radiology device
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Dec 2000
Decision
90d
Days
Class 2
Risk

K002782 is an FDA 510(k) clearance for the HERMES HD AQ ACQUISITION STATION AND HERMES 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 Nuclear Diagnostics AB (Beltsville, US). The FDA issued a Cleared decision on December 5, 2000 after a review of 90 days - within the typical 510(k) review window.

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 Nuclear Diagnostics AB devices

FDA 510(k) Submission Details - K002782

510(k) Number K002782 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received September 06, 2000
Decision Date December 05, 2000
Days to Decision 90 days
Submission Type Traditional
Review Panel Radiology (RA)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
17d faster than avg
Panel avg: 107d · This submission: 90d
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 1737
Devices cleared under the same product code (LLZ) and FDA review panel - the closest regulatory comparables to K002782.
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