Myflon Surgical Mask Level 3

FDA 510(k) K212111 · Feliks Plastik Laminasyon VE Ambalaj Malzemeleri Sanayi

Substantially Equivalent

510(k) numberK212111

Submission

Device name
Myflon Surgical Mask Level 3
Applicant
Feliks Plastik Laminasyon VE Ambalaj Malzemeleri Sanayi
Eskisehir, TR
Received
July 6, 2021
Decision date
January 23, 2022
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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K252964PRIMED Surgical and Procedure MasksFXX · Traditional Primed Medical Products, Inc.11/04/2025SE
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More from Winner Medical Co., Ltd.

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Questions and answers

When was Myflon Surgical Mask Level 3 cleared by the FDA?

Myflon Surgical Mask Level 3 (K212111) received a 510(k) decision of Substantially Equivalent on January 23, 2022, 201 days after the submission was received.

What is the product code of K212111?

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