GLOBAL TREASURES FLUID FILLED TEETHER
K-Number: K043033 · 2005-03-22
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Device Summary
Frequently Asked Questions
What is the GLOBAL TREASURES FLUID FILLED TEETHER?
GLOBAL TREASURES FLUID FILLED TEETHER is a medical device that received FDA 510(k) clearance on 2005-03-22. The listed applicant is Global Treasure Industries , Ltd.. The 510(k) number is K043033.
When did GLOBAL TREASURES FLUID FILLED TEETHER receive FDA 510(k) clearance?
GLOBAL TREASURES FLUID FILLED TEETHER received FDA 510(k) clearance on 2005-03-22, under 510(k) number K043033.
Who is the listed applicant for GLOBAL TREASURES FLUID FILLED TEETHER?
The FDA 510(k) record lists Global Treasure Industries , Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for GLOBAL TREASURES FLUID FILLED TEETHER?
The FDA product code for GLOBAL TREASURES FLUID FILLED 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 Global Treasure 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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