Portable Oxygen Concentrator

FDA 510(k) K252399 · Honsun (Nantong) Co., Ltd.

Substantially Equivalent

510(k) numberK252399

Submission

Device name
Portable Oxygen Concentrator
Applicant
Honsun (Nantong) Co., Ltd.
Nantong, CN
Received
July 31, 2025
Decision date
June 17, 2026
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
CAW – Generator, Oxygen, Portable
Device class
Class II (moderate risk)
Regulation
21 CFR 868.5440
Specialty
Anesthesiology

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Questions and answers

When was Portable Oxygen Concentrator cleared by the FDA?

Portable Oxygen Concentrator (K252399) received a 510(k) decision of Substantially Equivalent on June 17, 2026, 321 days after the submission was received.

What is the product code of K252399?

The FDA product code is CAW – Generator, Oxygen, Portable, a Class II (moderate risk) device regulated under 21 CFR 868.5440.