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FDA 510(k)

Apex Locator

K-Number: K231990 · 2024-02-13

ApplicantCefla S.C.
Decision Date2024-02-13
Product CodeLQY
DecisionSubstantially Equivalent

Device Summary

Apex Locator is the device name listed in this FDA 510(k) record. The listed applicant is Cefla S.C.. It received FDA 510(k) clearance on 2024-02-13 under 510(k) number K231990. The device is classified under product code LQY. FDA Decision: Substantially Equivalent.

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.

View all 15 devices →

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.