Cleared Traditional

K243244 - Heated Breathing Tube (FDA 510(k) Clearance)

Jul 2025
Decision
287d
Days
Class 2
Risk

K243244 is an FDA 510(k) clearance for the Heated Breathing Tube. This device is classified as a Heater, Breathing System W/wo Controller (not Humidifier Or Nebulizer (Class II - Special Controls, product code BZE).

Submitted by Guangdong Eda Technology Co., Ltd. (Guangdong Province, CN). The FDA issued a Cleared decision on July 25, 2025, 287 days after receiving the submission on October 11, 2024.

This device falls under the Anesthesiology FDA review panel. Regulated under 21 CFR 868.5270.

Submission Details

510(k) Number K243244 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received October 11, 2024
Decision Date July 25, 2025
Days to Decision 287 days
Submission Type Traditional
Review Panel Anesthesiology (AN)
Summary Summary PDF

Device Classification

Product Code BZE - Heater, Breathing System W/wo Controller (not Humidifier Or Nebulizer
Device Class Class II - Special Controls
CFR Regulation 21 CFR 868.5270

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