X-Clever
K-Number: K212137 · 2021-12-10
Device Summary
Frequently Asked Questions
What is the X-Clever?
X-Clever is a medical device that received FDA 510(k) clearance on 2021-12-10. The listed applicant is Lg Electronics.Inc. The 510(k) number is K212137.
When did X-Clever receive FDA 510(k) clearance?
X-Clever received FDA 510(k) clearance on 2021-12-10, under 510(k) number K212137.
Who is the listed applicant for X-Clever?
The FDA 510(k) record lists Lg Electronics.Inc as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for X-Clever?
The FDA product code for X-Clever is LLZ.
Other records listing Lg Electronics.Inc 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: LLZ)
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.