Cleared Traditional

K140984 - TANGO3 WATER STORAGE TANK WITH OZONE DISINFECTION SYSTEM

K140984 is an FDA 510(k) clearance for TANGO3 WATER STORAGE TANK WITH OZONE DI..., manufactured by Tango3, LLC. The device is a Class 2 Gastroenterology & Urology device with product code FIN cleared through the Traditional 510(k) pathway after a 271-day FDA review.

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Jan 2015
Decision
271d
Days
Class 2
Risk

K140984 is an FDA 510(k) clearance for the TANGO3 WATER STORAGE TANK WITH OZONE DISINFECTION SYSTEM. Classified as Tank, Holding, Dialysis (product code FIN), Class II - Special Controls.

Submitted by Tango3, LLC (Simpsonville, US). The FDA issued a Cleared decision on January 12, 2015 after a review of 271 days - an extended review cycle.

This device falls under the Gastroenterology & Urology FDA review panel, regulated under 21 CFR 876.5820 - 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 Tango3, LLC devices

FDA 510(k) Submission Details - K140984

510(k) Number K140984 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received April 16, 2014
Decision Date January 12, 2015
Days to Decision 271 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
140d slower than avg
Panel avg: 131d · This submission: 271d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

FIN Device Classification - Class 2, Special Controls

Product Code FIN Tank, Holding, Dialysis
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 876.5820
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 - FIN Tank, Holding, Dialysis

All 11
Devices cleared under the same product code (FIN) and FDA review panel - the closest regulatory comparables to K140984.
AMERIWATER OZONE DISINFECTION SYSTEM
K141213 · Ameriwater · Dec 2014
BICARB MIXING AND DISTRIBUTION SYSTEM
K112427 · Isopure, Corp. · Jan 2012
TANGO3 WATER STORAGE TANK WITH OZONE DISINFECTION SYSTEM
K093641 · Tango3, LLC · Dec 2010
DIALYSIS SERVICES, INC., TYPHOON BICARB MIXING AND DISTRIBUTION SYSTEM
K060333 · Dialysis Services, Inc. · Sep 2006
AMERIWATER SOLUTION MIX AND DISTRIBUTION SYSTEM FOR HEMODIALYSIS
K051031 · Ameriwater · Jan 2006
PURE WATER, INC.'S BICARB MIX, STORAGE AND DISTRIBUTION SYSTEM
K993272 · Pure Water, Inc. · Apr 2000