Cleared Traditional

K132353 - SUCTION LIPOPLASTY ACCESSORIES

K132353 is an FDA 510(k) clearance for SUCTION LIPOPLASTY ACCESSORIES, manufactured by Inex. The device is a Class 2 General & Plastic Surgery device with product code QPB cleared through the Traditional 510(k) pathway after a 366-day FDA review.

K132353 · Inex · General & Plastic Surgery device
Download Printable Device Report (PDF) Official FDA 510(k) Summary (PDF)
Optimized for regulatory review, auditing and printing
Jul 2014
Decision
366d
Days
Class 2
Risk

K132353 is an FDA 510(k) clearance for the SUCTION LIPOPLASTY ACCESSORIES. Classified as System, Suction, Lipoplasty For Removal (product code QPB), Class II - Special Controls.

Submitted by Inex (Puiseux Le Hauberger, FR). The FDA issued a Cleared decision on July 30, 2014 after a review of 366 days - an unusually long review period, suggesting complex equivalence evaluation.

This device falls under the General & Plastic Surgery FDA review panel, regulated under 21 CFR 878.5040 - the FDA general and plastic surgery 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. Elevated predicate reliance profile. This clearance follows a standard predicate-based equivalence path within the General & Plastic Surgery review framework, consistent with the majority of Class II 510(k) submissions.

FDA 510(k) Submission Details - K132353

510(k) Number K132353 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received July 29, 2013
Decision Date July 30, 2014
Days to Decision 366 days
Submission Type Traditional
Review Panel General & Plastic Surgery (SU)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
251d slower than avg
Panel avg: 115d · This submission: 366d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

QPB Device Classification - Class 2, Special Controls

Product Code QPB System, Suction, Lipoplasty For Removal
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 878.5040
Definition A Suction Lipoplasty System Is A Device Intended For The Removal Of Adipose Tissue For Purposes Of Aesthetic Body Contouring
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 General & Plastic Surgery devices follow this clearance model.

Regulatory Peers - QPB System, Suction, Lipoplasty For Removal

All 59
Devices cleared under the same product code (QPB) and FDA review panel - the closest regulatory comparables to K132353.
Basic, Dominant Flex
K170329 · Modela AG · Mar 2017
VITRUVIAN ULTIMATE ASPIRATOR
K161722 · Black & Black Surgical, Inc. · Jul 2016
Basic, Dominant Flex, KV-6
K150134 · Medela AG · Apr 2015
HYDRASOLVE CONSOLE STERILE TREATMENT KIT REUSABLE CANNULA, 4MM DIA, 26 CM LENGTH, 3 APERTURE REUSABLE CANNULA, 4MM DIA,
K121218 · Andrew Technologies, LLC · Dec 2012
MICROAIRE SURGICAL INSTRUMENTS LLC
K113128 · Microaire Surgical Instruments, LLC · Aug 2012
SUCTION LIPOLASTY ACCESSORIES
K113795 · Norman M. Black Iii · Aug 2012
K132353 · SUCTION LIPOPLASTY ACCESSORIES
Download PDF FDA Summary Inex