21HQ613D
K-Number: K221061 · 2022-06-03
ApplicantLg Electronics.Inc
Decision Date2022-06-03
Product CodePGY
Advisory CommitteeRA
DecisionSubstantially Equivalent
Device Summary
21HQ613D is a medical device manufactured by Lg Electronics.Inc. It received FDA 510(k) clearance on 2022-06-03 under approval number K221061. The device is classified under product code PGY. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the 21HQ613D?
21HQ613D is a medical device that received FDA 510(k) clearance on 2022-06-03. It is manufactured by Lg Electronics.Inc. The 510(k) number is K221061.
When was 21HQ613D approved by the FDA?
21HQ613D received FDA 510(k) clearance on 2022-06-03, under approval number K221061.
What company makes 21HQ613D?
21HQ613D is manufactured by Lg Electronics.Inc.
What is the FDA product code for 21HQ613D?
The FDA product code for 21HQ613D is PGY.
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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.