Cleared Traditional

K260251 - BreathCare PAP III (YH-390N)

K260251 is an FDA 510(k) clearance for BreathCare PAP III (YH-390N), manufactured by Suzhou Yuyue Medical Technology Co., Ltd.. The device is a Class 2 Anesthesiology device with product code BZD cleared through the Traditional 510(k) pathway after a 269-day FDA review.

K260251 · Suzhou Yuyue Medical Technology Co., Ltd. · Anesthesiology device
Download Printable Device Report (PDF) Official FDA 510(k) Summary (PDF)
Optimized for regulatory review, auditing and printing
Oct 2026
Decision
269d
Days
Class 2
Risk

K260251 is an FDA 510(k) clearance for the BreathCare PAP III (YH-390N). Classified as Ventilator, Non-continuous (respirator) (product code BZD), Class II - Special Controls.

Submitted by Suzhou Yuyue Medical Technology Co., Ltd. (Suzhou, CN). The FDA issued a Cleared decision on October 23, 2026 after a review of 269 days - an extended review cycle.

This device falls under the Anesthesiology FDA review panel, regulated under 21 CFR 868.5905 - 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. This clearance follows a standard predicate-based equivalence path within the Anesthesiology review framework, consistent with the majority of Class II 510(k) submissions.

FDA 510(k) Submission Details - K260251

510(k) Number K260251 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received January 27, 2026
Decision Date October 23, 2026
Days to Decision 269 days
Submission Type Traditional
Review Panel Anesthesiology (AN)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
129d slower than avg
Panel avg: 140d · This submission: 269d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

BZD Device Classification - Class 2, Special Controls

Product Code BZD Ventilator, Non-continuous (respirator)
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 868.5905
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 - BZD Ventilator, Non-continuous (respirator)

All 462
Devices cleared under the same product code (BZD) and FDA review panel - the closest regulatory comparables to K260251.
Altis Full Face Mask
K261262 · Respironics, Inc. · Sep 2026
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K253166 · BMC Medical Co., Ltd. · Apr 2026
K260251 · BreathCare PAP III (YH-390N)
Download PDF FDA Summary Suzhou Yuyue Medical …