FDA 510(k)

32HQ713D

K-Number: K223423 · 2023-03-01

Decision Date2023-03-01

Product CodePGY

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

32HQ713D is a medical device manufactured by Lg Electronics.Inc. It received FDA 510(k) clearance on 2023-03-01 under approval number K223423. 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 32HQ713D?

32HQ713D is a medical device that received FDA 510(k) clearance on 2023-03-01. It is manufactured by Lg Electronics.Inc. The 510(k) number is K223423.

When was 32HQ713D approved by the FDA?

32HQ713D received FDA 510(k) clearance on 2023-03-01, under approval number K223423.

What company makes 32HQ713D?

32HQ713D is manufactured by Lg Electronics.Inc.

What is the FDA product code for 32HQ713D?

The FDA product code for 32HQ713D 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.