Cleared Traditional

K060166 - OHMEGA

K060166 is an FDA 510(k) clearance for OHMEGA, manufactured by Medical Measurement Systems B.V.. The device is a Class 2 Gastroenterology & Urology device with product code FFX cleared through the Traditional 510(k) pathway after a 88-day FDA review.

K060166 · Medical Measurement Systems B.V. · Gastroenterology & Urology device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Apr 2006
Decision
88d
Days
Class 2
Risk

K060166 is an FDA 510(k) clearance for the OHMEGA. Classified as System, Gastrointestinal Motility (electrical) (product code FFX), Class II - Special Controls.

Submitted by Medical Measurement Systems B.V. (Enschede Overijssel, NL). The FDA issued a Cleared decision on April 21, 2006 after a review of 88 days - a notably fast clearance cycle.

This device falls under the Gastroenterology & Urology FDA review panel, regulated under 21 CFR 876.1725 - the FDA gastroenterology and urology device 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 Medical Measurement Systems B.V. devices

FDA 510(k) Submission Details - K060166

510(k) Number K060166 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received January 23, 2006
Decision Date April 21, 2006
Days to Decision 88 days
Submission Type Traditional
Review Panel Gastroenterology & Urology (GU)
Summary Statement
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
43d faster than avg
Panel avg: 131d · This submission: 88d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

FFX Device Classification - Class 2, Special Controls

Product Code FFX System, Gastrointestinal Motility (electrical)
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 876.1725
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 Gastroenterology & Urology devices follow this clearance model.

Regulatory Peers - FFX System, Gastrointestinal Motility (electrical)

All 52
Devices cleared under the same product code (FFX) and FDA review panel - the closest regulatory comparables to K060166.
ANORECTAL MANOMETRY SOFTWARE OPTION ARM-1
K082056 · Life-Tech, Inc. · Nov 2008
MODIFICATION TO SOLAR GI
K071094 · Medical Measurement Systems B.V. · Aug 2007
UNITIP HIGH RESOLUTION CATHETER
K062222 · Unisensor AG · Mar 2007
SOLAR GI
K052338 · Medical Measurement Systems B.V. · Dec 2005
INSIGHT, MODEL S980000
K012232 · Sandhill Scientific, Inc. · Jun 2002
SANDHILL UNITIP CATHETER PRESSURE SENSOR, MODEL K 5251-L3-0026
K002427 · Sandhill Scientific, Inc. · Jun 2001