21HQ613D
K-Number: K221061 · 2022-06-03
Device Summary
Frequently Asked Questions
What is the 21HQ613D?
21HQ613D is a medical device that received FDA 510(k) clearance on 2022-06-03. The listed applicant is Lg Electronics.Inc. The 510(k) number is K221061.
When did 21HQ613D receive FDA 510(k) clearance?
21HQ613D received FDA 510(k) clearance on 2022-06-03, under 510(k) number K221061.
Who is the listed applicant for 21HQ613D?
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 21HQ613D?
The FDA product code for 21HQ613D 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.