Propex IQ Apex Locator
K-Number: K191806 · 2019-10-03
Device Summary
Propex IQ Apex Locator is a medical device manufactured by Dentsply Sirona. It received FDA 510(k) clearance on 2019-10-03 under approval number K191806. The device is classified under product code LQY. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Propex IQ Apex Locator?
Propex IQ Apex Locator is a medical device that received FDA 510(k) clearance on 2019-10-03. It is manufactured by Dentsply Sirona. The 510(k) number is K191806.
When was Propex IQ Apex Locator approved by the FDA?
Propex IQ Apex Locator received FDA 510(k) clearance on 2019-10-03, under approval number K191806.
What company makes Propex IQ Apex Locator?
Propex IQ Apex Locator is manufactured by Dentsply Sirona.
What is the FDA product code for Propex IQ Apex Locator?
The FDA product code for Propex IQ Apex Locator is LQY.
Other Devices by Dentsply Sirona
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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.