Cleared Traditional

K071134 - SONOSITE MAXX SERIES DIAGNOSTIC ULTRASO...

K071134 is an FDA 510(k) clearance for SONOSITE MAXX SERIES DIAGNOSTIC ULTRASO..., manufactured by Sonosite,Inc.. The device is a Class 2 Radiology device with product code IYO cleared through the Traditional 510(k) pathway after a 15-day FDA review.

K071134 · Sonosite,Inc. · Radiology device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
May 2007
Decision
15d
Days
Class 2
Risk

K071134 is an FDA 510(k) clearance for the SONOSITE MAXX SERIES DIAGNOSTIC ULTRASOUND SYSTEM. Classified as System, Imaging, Pulsed Echo, Ultrasonic (product code IYO), Class II - Special Controls.

Submitted by Sonosite,Inc. (Bothell, US). The FDA issued a Cleared decision on May 8, 2007 after a review of 15 days - a notably fast clearance cycle.

This device falls under the Radiology FDA review panel, regulated under 21 CFR 892.1560 - 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 Sonosite,Inc. devices

FDA 510(k) Submission Details - K071134

510(k) Number K071134 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received April 23, 2007
Decision Date May 08, 2007
Days to Decision 15 days
Submission Type Traditional
Review Panel Radiology (RA)
Summary Summary PDF
Third-party Review Yes - reviewed by an FDA-accredited third party
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
92d faster than avg
Panel avg: 107d · This submission: 15d
Pathway characteristics
Predicate-based equivalence. No clinical trials required. Third-party reviewed.

IYO Device Classification - Class 2, Special Controls

Product Code IYO System, Imaging, Pulsed Echo, Ultrasonic
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 892.1560
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 Consultant

Regulatory Technology Services, LLC
MARK JOB

The regulatory consultant manages the 510(k) submission process on behalf of the applicant - coordinating technical documentation, predicate strategy and FDA communications. Identifying the consultant behind a submission is a key signal for competitive regulatory intelligence.

Regulatory Peers - IYO System, Imaging, Pulsed Echo, Ultrasonic

All 448
Devices cleared under the same product code (IYO) and FDA review panel - the closest regulatory comparables to K071134.
MYLAB30, MODEL 7300
K071996 · Esaote, S.P.A. · Aug 2007
SONOLINE G20 DIAGNOSTIC ULTRASOUND SYSTEMS
K071314 · Siemens Medical Solutions USA, Inc. · May 2007
SITE-RITE 6 ULTRASOUND SYSTEM, MODEL SITE-RITE 6
K071204 · C.R. Bard, Inc. · May 2007
DP-9900 DIGITAL ULTRASONIC DIAGNOSTIC IMAGING SYSTEM
K070526 · Shenzhen Mindray Bio-Medical Electronics Co., Ltd. · Mar 2007
MODIFICATION TO ACUSON SEQUOIA ULTRASOUND SYSTEM
K063085 · Siemens Medical Solutions USA, Inc. · Nov 2006
VOLCANO S51 FAMILY OF IMAGING SYSTEMS
K061215 · Volcano Corporation · Aug 2006