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FDA 510(k)

Procedure mask/Surgical mask/Face mask

K-Number: K223232 · 2023-03-06

Decision Date2023-03-06
Product CodeFXX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

Procedure mask/Surgical mask/Face mask is a medical device manufactured by Winner Medical Co., Ltd.. It received FDA 510(k) clearance on 2023-03-06 under approval number K223232. The device is classified under product code FXX. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Procedure mask/Surgical mask/Face mask?

Procedure mask/Surgical mask/Face mask is a medical device that received FDA 510(k) clearance on 2023-03-06. It is manufactured by Winner Medical Co., Ltd.. The 510(k) number is K223232.

When was Procedure mask/Surgical mask/Face mask approved by the FDA?

Procedure mask/Surgical mask/Face mask received FDA 510(k) clearance on 2023-03-06, under approval number K223232.

What company makes Procedure mask/Surgical mask/Face mask?

Procedure mask/Surgical mask/Face mask is manufactured by Winner Medical Co., Ltd..

What is the FDA product code for Procedure mask/Surgical mask/Face mask?

The FDA product code for Procedure mask/Surgical mask/Face mask is FXX.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.