21HQ513D
K-Number: K223789 · 2023-01-09
Device Summary
Frequently Asked Questions
What is the 21HQ513D?
21HQ513D is a medical device that received FDA 510(k) clearance on 2023-01-09. The listed applicant is Lg Electronics.Inc. The 510(k) number is K223789.
When did 21HQ513D receive FDA 510(k) clearance?
21HQ513D received FDA 510(k) clearance on 2023-01-09, under 510(k) number K223789.
Who is the listed applicant for 21HQ513D?
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 21HQ513D?
The FDA product code for 21HQ513D is PGY.
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: PGY)
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.