21HQ513D
K-Number: K223789 · 2023-01-09
ApplicantLg Electronics.Inc
Decision Date2023-01-09
Product CodePGY
Advisory CommitteeRA
DecisionSubstantially Equivalent
Device Summary
21HQ513D is a medical device manufactured by Lg Electronics.Inc. It received FDA 510(k) clearance on 2023-01-09 under approval number K223789. 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 21HQ513D?
21HQ513D is a medical device that received FDA 510(k) clearance on 2023-01-09. It is manufactured by Lg Electronics.Inc. The 510(k) number is K223789.
When was 21HQ513D approved by the FDA?
21HQ513D received FDA 510(k) clearance on 2023-01-09, under approval number K223789.
What company makes 21HQ513D?
21HQ513D is manufactured by Lg Electronics.Inc.
What is the FDA product code for 21HQ513D?
The FDA product code for 21HQ513D 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.