Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR, NMPA) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

Surgical Masks, Model:FE-1

K-Number: K210767 · 2021-06-10

Decision Date2021-06-10
Product CodeFXX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

Surgical Masks, Model:FE-1 is a medical device manufactured by Hunan Triplex Precision Medical Devices Co., Ltd.. It received FDA 510(k) clearance on 2021-06-10 under approval number K210767. 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 Masks, Model:FE-1?

Surgical Masks, Model:FE-1 is a medical device that received FDA 510(k) clearance on 2021-06-10. It is manufactured by Hunan Triplex Precision Medical Devices Co., Ltd.. The 510(k) number is K210767.

When was Surgical Masks, Model:FE-1 approved by the FDA?

Surgical Masks, Model:FE-1 received FDA 510(k) clearance on 2021-06-10, under approval number K210767.

What company makes Surgical Masks, Model:FE-1?

Surgical Masks, Model:FE-1 is manufactured by Hunan Triplex Precision Medical Devices Co., Ltd..

What is the FDA product code for Surgical Masks, Model:FE-1?

The FDA product code for Surgical Masks, Model:FE-1 is FXX.

Related Clinical Trials

Related Devices (Code: FXX)

Official Source

View on FDA Database →

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