FDA 510(k)

31HN713D

K-Number: K201777 · 2020-10-08

Decision Date2020-10-08

Product CodePGY

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

31HN713D is a medical device manufactured by Lg Electronics.Inc. It received FDA 510(k) clearance on 2020-10-08 under approval number K201777. 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 31HN713D?

31HN713D is a medical device that received FDA 510(k) clearance on 2020-10-08. It is manufactured by Lg Electronics.Inc. The 510(k) number is K201777.

When was 31HN713D approved by the FDA?

31HN713D received FDA 510(k) clearance on 2020-10-08, under approval number K201777.

What company makes 31HN713D?

31HN713D is manufactured by Lg Electronics.Inc.

What is the FDA product code for 31HN713D?

The FDA product code for 31HN713D 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.