FDA 510(k)

32HL512D, 31HN713D, 32HQ713D

K-Number: K230845 · 2023-04-27

Decision Date2023-04-27

Product CodePGY

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

32HL512D, 31HN713D, 32HQ713D is a medical device manufactured by Lg Electronics.Inc. It received FDA 510(k) clearance on 2023-04-27 under approval number K230845. 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 32HL512D, 31HN713D, 32HQ713D?

32HL512D, 31HN713D, 32HQ713D is a medical device that received FDA 510(k) clearance on 2023-04-27. It is manufactured by Lg Electronics.Inc. The 510(k) number is K230845.

When was 32HL512D, 31HN713D, 32HQ713D approved by the FDA?

32HL512D, 31HN713D, 32HQ713D received FDA 510(k) clearance on 2023-04-27, under approval number K230845.

What company makes 32HL512D, 31HN713D, 32HQ713D?

32HL512D, 31HN713D, 32HQ713D is manufactured by Lg Electronics.Inc.

What is the FDA product code for 32HL512D, 31HN713D, 32HQ713D?

The FDA product code for 32HL512D, 31HN713D, 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.