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FDA 510(k)

24HR513C

K-Number: K232985 · 2023-12-11

Decision Date2023-12-11
Product CodePGY
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

24HR513C is the device name listed in this FDA 510(k) record. The listed applicant is Lg Electronics.Inc. It received FDA 510(k) clearance on 2023-12-11 under 510(k) number K232985. 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 24HR513C?

24HR513C is a medical device that received FDA 510(k) clearance on 2023-12-11. The listed applicant is Lg Electronics.Inc. The 510(k) number is K232985.

When did 24HR513C receive FDA 510(k) clearance?

24HR513C received FDA 510(k) clearance on 2023-12-11, under 510(k) number K232985.

Who is the listed applicant for 24HR513C?

The FDA 510(k) record lists Lg Electronics.Inc as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for 24HR513C?

The FDA product code for 24HR513C is PGY.

Other records listing Lg Electronics.Inc as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

View all 32 devices →

Related Devices (Code: PGY)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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.