Cleared Traditional

K202354 - Surgical Mask-Model Number CW01 (FDA 510(k) Clearance)

Sep 2020
Decision
20d
Days
Class 2
Risk

K202354 is an FDA 510(k) clearance for the Surgical Mask-Model Number CW01. This device is classified as a Mask, Surgical (Class II - Special Controls, product code FXX).

Submitted by Hunan Heng Chang Pharmaceutical Co., Ltd. (Changsha, CN). The FDA issued a Cleared decision on September 8, 2020, 20 days after receiving the submission on August 19, 2020.

This device falls under the General Hospital FDA review panel. Regulated under 21 CFR 878.4040.

Submission Details

510(k) Number K202354 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received August 19, 2020
Decision Date September 08, 2020
Days to Decision 20 days
Submission Type Traditional
Review Panel General Hospital (HO)
Summary Summary PDF

Device Classification

Product Code FXX - Mask, Surgical
Device Class Class II - Special Controls
CFR Regulation 21 CFR 878.4040

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