Cleared Traditional

K002051 - INVIDOS

K002051 is an FDA 510(k) clearance for INVIDOS, manufactured by Scanditronix Medical AB. The device is a Class 2 Radiology device with product code IYE cleared through the Traditional 510(k) pathway after a 61-day FDA review.

K002051 · Scanditronix Medical AB · Radiology device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Sep 2000
Decision
61d
Days
Class 2
Risk

K002051 is an FDA 510(k) clearance for the INVIDOS. Classified as Accelerator, Linear, Medical (product code IYE), Class II - Special Controls.

Submitted by Scanditronix Medical AB (Uppsala S-754 50, SE). The FDA issued a Cleared decision on September 5, 2000 after a review of 61 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 Scanditronix Medical AB devices

FDA 510(k) Submission Details - K002051

510(k) Number K002051 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received July 06, 2000
Decision Date September 05, 2000
Days to Decision 61 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
46d faster than avg
Panel avg: 107d · This submission: 61d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

IYE Device Classification - Class 2, Special Controls

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 442
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ECLIPSE 6.5
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