Apex Locator, DPEX III
K-Number: K181087 · 2018-12-18
Device Summary
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. The listed applicant is Guilin Woodpecker Medical Instrument Co., Ltd.. The 510(k) number is K181087.
When did Apex Locator, DPEX III receive FDA 510(k) clearance?
Apex Locator, DPEX III received FDA 510(k) clearance on 2018-12-18, under 510(k) number K181087.
Who is the listed applicant for Apex Locator, DPEX III?
The FDA 510(k) record lists Guilin Woodpecker Medical Instrument Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Apex Locator, DPEX III?
The FDA product code for Apex Locator, DPEX III is LQY.
Other records listing Guilin Woodpecker Medical Instrument 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.