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FDA 510(k)

WATER FILLED TEETHER

K-Number: K052105 · 2005-10-31

Decision Date2005-10-31
Product CodeKKO
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

WATER FILLED TEETHER is the device name listed in this FDA 510(k) record. The listed applicant is Royal Industries (Thailand) Public Co. , Ltd.. It received FDA 510(k) clearance on 2005-10-31 under 510(k) number K052105. The device is classified under product code KKO. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

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

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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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