FU HONG INDUSTRIES LIMITED SOOTHER TEETHER
K-Number: K093370 · 2010-01-21
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Device Summary
Frequently Asked Questions
What is the FU HONG INDUSTRIES LIMITED SOOTHER TEETHER?
FU HONG INDUSTRIES LIMITED SOOTHER TEETHER is a medical device that received FDA 510(k) clearance on 2010-01-21. The listed applicant is Fu Hong Industries , Ltd.. The 510(k) number is K093370.
When did FU HONG INDUSTRIES LIMITED SOOTHER TEETHER receive FDA 510(k) clearance?
FU HONG INDUSTRIES LIMITED SOOTHER TEETHER received FDA 510(k) clearance on 2010-01-21, under 510(k) number K093370.
Who is the listed applicant for FU HONG INDUSTRIES LIMITED SOOTHER TEETHER?
The FDA 510(k) record lists Fu Hong Industries , Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for FU HONG INDUSTRIES LIMITED SOOTHER TEETHER?
The FDA product code for FU HONG INDUSTRIES LIMITED SOOTHER TEETHER is KKO.
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 Fu Hong Industries , 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: KKO)
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
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
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