Cleared Traditional

K151959 - AirLife Infant Single Limb Heated Wire ...

K151959 is an FDA 510(k) clearance for AirLife Infant Single Limb Heated Wire ..., manufactured by Carefusion, Inc.. The device is a Class 2 Anesthesiology device with product code BZE cleared through the Traditional 510(k) pathway after a 188-day FDA review.

K151959 · Carefusion, Inc. · Anesthesiology device
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Jan 2016
Decision
188d
Days
Class 2
Risk

K151959 is an FDA 510(k) clearance for the AirLife Infant Single Limb Heated Wire Circuit. Classified as Heater, Breathing System W/wo Controller (not Humidifier Or Nebulizer within the BZE classification (a category for neonatal and pediatric respiratory circuit components), Class II - Special Controls.

Submitted by Carefusion, Inc. (Vernon Hills, US). The FDA issued a Cleared decision on January 20, 2016 after a review of 188 days - an extended review cycle.

This device falls under the Anesthesiology FDA review panel, regulated under 21 CFR 868.5270 - the FDA anesthesiology and respiratory 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. Neonatal respiratory circuit components typically face extended FDA review due to heightened safety scrutiny for pediatric patient populations - the 176-day cycle reflects this additional regulatory diligence.

View all Carefusion, Inc. devices

FDA 510(k) Submission Details - K151959

510(k) Number K151959 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received July 16, 2015
Decision Date January 20, 2016
Days to Decision 188 days
Submission Type Traditional
Review Panel Anesthesiology (AN)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
48d slower than avg
Panel avg: 140d · This submission: 188d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

BZE Device Classification - Class 2, Special Controls

Product Code BZE Heater, Breathing System W/wo Controller (not Humidifier Or Nebulizer
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 868.5270
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 Anesthesiology devices follow this clearance model.

Regulatory Peers - BZE Heater, Breathing System W/wo Controller (not Humidifier Or Nebulizer

All 24
Devices cleared under the same product code (BZE) and FDA review panel - the closest regulatory comparables to K151959.
Sunset Heated CPAP Tube
K201418 · Sunset Healthcare Solutions, Inc. · Jan 2021
Neonatal ConchaSmart Breathing Circuits
K173280 · Teleflexmedical, Inc. · Aug 2018
AirLife Infant Heated Wire Circuit
K151303 · Care Fusion · Jan 2016
RESPIRONICS REUSABLE HEATED TUBING
K140424 · Respironics, Inc. · Nov 2014
ADULT EVAQUA 2' DUAL HEATED BREATHING CIRCUITS
K122432 · Fisher &Paykel Healthcare , Ltd. · Dec 2012
DUAL HEATED INFANT VREATHING CIROUITS
K103767 · Fisher &Paykel Healthcare , Ltd. · Apr 2012