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FDA 510(k)

Surgical Face Mask

K-Number: K212913 · 2022-01-14

Decision Date2022-01-14
Product CodeFXX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

Surgical Face Mask is the device name listed in this FDA 510(k) record. The listed applicant is Jiangxi Ganlong Pharmaceutical Co., Ltd.. It received FDA 510(k) clearance on 2022-01-14 under 510(k) number K212913. 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 Surgical Face Mask?

Surgical Face Mask is a medical device that received FDA 510(k) clearance on 2022-01-14. The listed applicant is Jiangxi Ganlong Pharmaceutical Co., Ltd.. The 510(k) number is K212913.

When did Surgical Face Mask receive FDA 510(k) clearance?

Surgical Face Mask received FDA 510(k) clearance on 2022-01-14, under 510(k) number K212913.

Who is the listed applicant for Surgical Face Mask?

The FDA 510(k) record lists Jiangxi Ganlong Pharmaceutical Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Surgical Face Mask?

The FDA product code for Surgical Face Mask is FXX.

Related Devices (Code: FXX)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Official Source

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