nPro Surgical Mask

FDA 510(k) K203265 · Np Medical, Inc.

Substantially Equivalent

510(k) numberK203265

Submission

Device name
nPro Surgical Mask
Applicant
Np Medical, Inc.
Clinton, MA, US
Received
November 5, 2020
Decision date
February 9, 2021
Decision
Substantially Equivalent (SESE)
Type
Abbreviated 510(k)
Summary
510(k) summary available from FDA
Third-party review
Yes

Official FDA 510(k) record

Device classification

Product code
FXX – Mask, Surgical
Device class
Class II (moderate risk)
Regulation
21 CFR 878.4040
Specialty
General, Plastic Surgery

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K252534Surgical Face Mask (Ear mount)FXX · Traditional Zhejiang Hangkang Medical Equipment Co., Ltd.03/03/2026SE
K253398Disposable Surgical Mask (Non-Sterile) (EFX3PLBLKMSK300)FXX · Special Efofex, Inc.02/19/2026SE
K252830Disposable Surgical Face Mask (3P00B, C2900)FXX · Traditional Beatles Medical Supplies (Xiantao) Co., Ltd.01/12/2026SE
K252650Disposable Medical Face MaskFXX · Traditional Makrite Industries, Inc.01/05/2026SE
K243342KP Protective Face MaskFXX · Traditional Kp Trading Co., Ltd.12/22/2025SE
K252941HALYARD* Adult Face Mask with SO SOFT* Lining and SO SOFT* EarloopsFXX · Traditional O&M Halyard, Inc.12/11/2025SE
K252964PRIMED Surgical and Procedure MasksFXX · Traditional Primed Medical Products, Inc.11/04/2025SE
K251902Vitaform Procedural Mask - Blue (Vitaform Blue); Vitaform Procedural Mask with Shield…FXX · Traditional Vitacore Industries, Inc.09/17/2025SE
K250082Procedure mask/Surgical mask/Face maskFXX · Traditional Winner Medical Co., Ltd.06/18/2025SE

More from Winner Medical Co., Ltd.

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K221518NP Medical nCompass Extension Set with Stabilizing BaseFPA · Traditional 11/03/2022SE
K130023K100 Neutral Displacement Needle Free ConnectorFPA · Traditional 04/03/2013SE
K973916NP Medical Capless Luer Activated ValveFPA · Traditional 03/09/1998SE

Questions and answers

When was nPro Surgical Mask cleared by the FDA?

nPro Surgical Mask (K203265) received a 510(k) decision of Substantially Equivalent on February 9, 2021, 96 days after the submission was received.

What is the product code of K203265?

The FDA product code is FXX – Mask, Surgical, a Class II (moderate risk) device regulated under 21 CFR 878.4040.