Cleared Traditional

K082142 - ACUSON S2000 DIAGNOSTIC ULTRASOUND SYSTEM

K082142 is an FDA 510(k) clearance for ACUSON S2000 DIAGNOSTIC ULTRASOUND SYSTEM, manufactured by Siemens Medical Solutions USA, Inc., Ultrasound DI. The device is a Class 2 Radiology device with product code IYN cleared through the Traditional 510(k) pathway after a 106-day FDA review.

K082142 · Siemens Medical Solutions USA, Inc., Ultrasound DI · Radiology device
Download Printable Device Report (PDF) Official FDA 510(k) Summary (PDF)
Optimized for regulatory review, auditing and printing
Nov 2008
Decision
106d
Days
Class 2
Risk

K082142 is an FDA 510(k) clearance for the ACUSON S2000 DIAGNOSTIC ULTRASOUND SYSTEM. Classified as System, Imaging, Pulsed Doppler, Ultrasonic within the IYN classification (a category covering pulsed Doppler and ultrasound imaging systems), Class II - Special Controls.

Submitted by Siemens Medical Solutions USA, Inc., Ultrasound DI (Mountainview, US). The FDA issued a Cleared decision on November 13, 2008 after a review of 106 days - within the typical 510(k) review window.

This device falls under the Radiology FDA review panel, regulated under 21 CFR 892.1550 - 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: Standard predicate-based submission. Standard predicate reliance. This clearance follows a standard predicate-based equivalence path within the Radiology review framework, consistent with the majority of Class II 510(k) submissions.

FDA 510(k) Submission Details - K082142

510(k) Number K082142 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received July 30, 2008
Decision Date November 13, 2008
Days to Decision 106 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
1d faster than avg
Panel avg: 107d · This submission: 106d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

IYN Device Classification - Class 2, Special Controls

Product Code IYN System, Imaging, Pulsed Doppler, Ultrasonic
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 892.1550
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 - IYN System, Imaging, Pulsed Doppler, Ultrasonic

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K082142 · ACUSON S2000 DIAGNOSTIC ULTRASOUND SYSTEM
Download PDF FDA Summary Siemens Medical Solut…