Disposable Medical mask

FDA 510(k) K210302 · Anhui Jbh Medical Apparatus Co., Ltd.

Substantially Equivalent

510(k) numberK210302

Submission

Device name
Disposable Medical mask
Applicant
Anhui Jbh Medical Apparatus Co., Ltd.
Chuzhou, CN
Received
February 3, 2021
Decision date
May 14, 2021
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

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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K252650Disposable Medical Face MaskFXX · Traditional Makrite Industries, Inc.01/05/2026SE
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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

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Questions and answers

When was Disposable Medical mask cleared by the FDA?

Disposable Medical mask (K210302) received a 510(k) decision of Substantially Equivalent on May 14, 2021, 100 days after the submission was received.

What is the product code of K210302?

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