JUSTWO MODEL TME-601 ROOT APEX LOCATOR
K-Number: K022020 · 2002-07-02
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Device Summary
Frequently Asked Questions
What is the JUSTWO MODEL TME-601 ROOT APEX LOCATOR?
JUSTWO MODEL TME-601 ROOT APEX LOCATOR is a medical device that received FDA 510(k) clearance on 2002-07-02. The listed applicant is Toei Electric Co., Ltd.. The 510(k) number is K022020.
When did JUSTWO MODEL TME-601 ROOT APEX LOCATOR receive FDA 510(k) clearance?
JUSTWO MODEL TME-601 ROOT APEX LOCATOR received FDA 510(k) clearance on 2002-07-02, under 510(k) number K022020.
Who is the listed applicant for JUSTWO MODEL TME-601 ROOT APEX LOCATOR?
The FDA 510(k) record lists Toei Electric Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for JUSTWO MODEL TME-601 ROOT APEX LOCATOR?
The FDA product code for JUSTWO MODEL TME-601 ROOT APEX LOCATOR is LQY.
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 Toei Electric 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: LQY)
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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