Cleared Traditional

K052678 - AQ-830 SLIM BODY, BODY FAT MONITOR

K052678 is an FDA 510(k) clearance for AQ-830 SLIM BODY, manufactured by Limax Electronics Co., Ltd.. The device is a Class 2 Gastroenterology & Urology device with product code MNW cleared through the Traditional 510(k) pathway after a 90-day FDA review.

K052678 · Limax Electronics Co., Ltd. · Gastroenterology & Urology device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Dec 2005
Decision
90d
Days
Class 2
Risk

K052678 is an FDA 510(k) clearance for the AQ-830 SLIM BODY, BODY FAT MONITOR. Classified as Analyzer, Body Composition (product code MNW), Class II - Special Controls.

Submitted by Limax Electronics Co., Ltd. (Flagstaff, US). The FDA issued a Cleared decision on December 27, 2005 after a review of 90 days - within the typical 510(k) review window.

This device falls under the Gastroenterology & Urology FDA review panel, regulated under 21 CFR 870.2770 - 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: Standard predicate-based submission. Standard predicate reliance. This clearance follows a standard predicate-based equivalence path within the Gastroenterology & Urology review framework, consistent with the majority of Class II 510(k) submissions.

View all Limax Electronics Co., Ltd. devices

FDA 510(k) Submission Details - K052678

510(k) Number K052678 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received September 28, 2005
Decision Date December 27, 2005
Days to Decision 90 days
Submission Type Traditional
Review Panel Gastroenterology & Urology (GU)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
41d faster than avg
Panel avg: 131d · This submission: 90d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

MNW Device Classification - Class 2, Special Controls

Product Code MNW Analyzer, Body Composition
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 870.2770
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 - MNW Analyzer, Body Composition

All 65
Devices cleared under the same product code (MNW) and FDA review panel - the closest regulatory comparables to K052678.
BC100 BODY COMPOSITION ANALYSIS SYSTEM
K060552 · Athletic Iq, Inc. · May 2006
IMPEDIMED - BODY COMPOSITION ANALYZER, MODEL IMP SFB7
K052319 · Impedimed Pty , Ltd. · Apr 2006
BIODYNAMICS BIA 500 BIOMPEDANCE BODY COMPOSITION ANALYZER
K051675 · Biodynamics Corp. · Mar 2006
BIOSPACE BODY COMPOSITION ANALYZERS, MODELS INBODY 520, 720 AND S20
K052646 · Biospace Corporation Limited · Dec 2005
STAYHEALTHY BODY COMPOSITION ANALYZER, MODELS BC1 AND BC2
K052522 · Stayhealthy, Inc. · Dec 2005
SLIMMANAGER, MODEL SM-X, SM-E
K051589 · Aiia Communication, Inc. · Oct 2005