Apex Locator
K-Number: K231990 · 2024-02-13
Device Summary
Frequently Asked Questions
What is the Apex Locator?
Apex Locator is a medical device that received FDA 510(k) clearance on 2024-02-13. The listed applicant is Cefla S.C.. The 510(k) number is K231990.
When did Apex Locator receive FDA 510(k) clearance?
Apex Locator received FDA 510(k) clearance on 2024-02-13, under 510(k) number K231990.
Who is the listed applicant for Apex Locator?
The FDA 510(k) record lists Cefla S.C. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Apex Locator?
The FDA product code for 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 Cefla S.C. 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.