Apex Locator, DPEX III
K-Number: K181087 · 2018-12-18
Decision Date2018-12-18
Product CodeLQY
DecisionSubstantially Equivalent
Device Summary
Apex Locator, DPEX III is a medical device manufactured by Guilin Woodpecker Medical Instrument Co., Ltd.. It received FDA 510(k) clearance on 2018-12-18 under approval number K181087. The device is classified under product code LQY. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Apex Locator, DPEX III?
Apex Locator, DPEX III is a medical device that received FDA 510(k) clearance on 2018-12-18. It is manufactured by Guilin Woodpecker Medical Instrument Co., Ltd.. The 510(k) number is K181087.
When was Apex Locator, DPEX III approved by the FDA?
Apex Locator, DPEX III received FDA 510(k) clearance on 2018-12-18, under approval number K181087.
What company makes Apex Locator, DPEX III?
Apex Locator, DPEX III is manufactured by Guilin Woodpecker Medical Instrument Co., Ltd..
What is the FDA product code for Apex Locator, DPEX III?
The FDA product code for Apex Locator, DPEX III is LQY.
Other Devices by Guilin Woodpecker Medical Instrument Co., Ltd.
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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.