Cleared Special

K081859 - MODIFICATION TO ONEDOSE PATIENT DOSIMETRY SYSTEM

K081859 is an FDA 510(k) clearance for MODIFICATION TO ONEDOSE PATIENT DOSIMET..., manufactured by Sicel Technologies, Inc.. The device is a Class 2 Radiology device with product code IYE cleared through the Special 510(k) pathway after a 34-day FDA review.

K081859 · Sicel Technologies, Inc. · Radiology device
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Aug 2008
Decision
34d
Days
Class 2
Risk

K081859 is an FDA 510(k) clearance for the MODIFICATION TO ONEDOSE PATIENT DOSIMETRY SYSTEM. Classified as Accelerator, Linear, Medical (product code IYE), Class II - Special Controls.

Submitted by Sicel Technologies, Inc. (Morrisville, US). The FDA issued a Cleared decision on August 4, 2008 after a review of 34 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. As a Special 510(k), this submission covers a manufacturer modification to an existing cleared device rather than a new device introduction.

Device pattern: Iterative device modification. Low regulatory complexity profile. This Special 510(k) clearance confirms that the manufacturer's modifications remained within the established regulatory envelope of the original cleared device.

View all Sicel Technologies, Inc. devices

FDA 510(k) Submission Details - K081859

510(k) Number K081859 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received July 01, 2008
Decision Date August 04, 2008
Days to Decision 34 days
Submission Type Special
Review Panel Radiology (RA)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
73d faster than avg
Panel avg: 107d · This submission: 34d
Pathway characteristics
Modification to existing cleared device.

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

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