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FDA 510(k)

27HJ713S

K-Number: K170899 · 2017-05-30

Decision Date2017-05-30
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

27HJ713S is the device name listed in this FDA 510(k) record. The listed applicant is Lg Electronics. It received FDA 510(k) clearance on 2017-05-30 under 510(k) number K170899. The device is classified under product code GCJ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the 27HJ713S?

27HJ713S is a medical device that received FDA 510(k) clearance on 2017-05-30. The listed applicant is Lg Electronics. The 510(k) number is K170899.

When did 27HJ713S receive FDA 510(k) clearance?

27HJ713S received FDA 510(k) clearance on 2017-05-30, under 510(k) number K170899.

Who is the listed applicant for 27HJ713S?

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

What is the FDA product code for 27HJ713S?

The FDA product code for 27HJ713S is GCJ.

Other records listing Lg Electronics 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: GCJ)

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.