WATER FILLED TEETHER
K-Number: K052105 · 2005-10-31
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Device Summary
Frequently Asked Questions
What is the WATER FILLED TEETHER?
WATER FILLED TEETHER is a medical device that received FDA 510(k) clearance on 2005-10-31. The listed applicant is Royal Industries (Thailand) Public Co. , Ltd.. The 510(k) number is K052105.
When did WATER FILLED TEETHER receive FDA 510(k) clearance?
WATER FILLED TEETHER received FDA 510(k) clearance on 2005-10-31, under 510(k) number K052105.
Who is the listed applicant for WATER FILLED TEETHER?
The FDA 510(k) record lists Royal Industries (Thailand) Public Co. , Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for WATER FILLED TEETHER?
The FDA product code for WATER 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.
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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