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FDA 510(k)

SURGICAL FACE MASK

K-Number: K043199 · 2005-02-16

Decision Date2005-02-16
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 Hong YA Non-Woven Products Co., Ltd.. It received FDA 510(k) clearance on 2005-02-16 under 510(k) number K043199. 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 2005-02-16. The listed applicant is Hong YA Non-Woven Products Co., Ltd.. The 510(k) number is K043199.

When did SURGICAL FACE MASK receive FDA 510(k) clearance?

SURGICAL FACE MASK received FDA 510(k) clearance on 2005-02-16, under 510(k) number K043199.

Who is the listed applicant for SURGICAL FACE MASK?

The FDA 510(k) record lists Hong YA Non-Woven Products 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 Clinical Trials

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.

Other records listing Hong YA Non-Woven Products Co., Ltd. as applicant

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.

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

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