FDA 510(k)

32HL512D

K-Number: K192925 · 2020-03-13

Decision Date2020-03-13

Product CodePGY

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

32HL512D is a medical device manufactured by Lg Electronics.Inc. It received FDA 510(k) clearance on 2020-03-13 under approval number K192925. 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?

32HL512D is a medical device that received FDA 510(k) clearance on 2020-03-13. It is manufactured by Lg Electronics.Inc. The 510(k) number is K192925.

When was 32HL512D approved by the FDA?

32HL512D received FDA 510(k) clearance on 2020-03-13, under approval number K192925.

What company makes 32HL512D?

32HL512D is manufactured by Lg Electronics.Inc.

What is the FDA product code for 32HL512D?

The FDA product code for 32HL512D is PGY.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.