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FDA 510(k)

Lunit INSIGHT MMG

K-Number: K211678 · 2021-11-17

ApplicantLunit, Inc.
Decision Date2021-11-17
Product CodeQDQ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

Lunit INSIGHT MMG is the device name listed in this FDA 510(k) record. The listed applicant is Lunit, Inc.. It received FDA 510(k) clearance on 2021-11-17 under 510(k) number K211678. The device is classified under product code QDQ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Lunit INSIGHT MMG?

Lunit INSIGHT MMG is a medical device that received FDA 510(k) clearance on 2021-11-17. The listed applicant is Lunit, Inc.. The 510(k) number is K211678.

When did Lunit INSIGHT MMG receive FDA 510(k) clearance?

Lunit INSIGHT MMG received FDA 510(k) clearance on 2021-11-17, under 510(k) number K211678.

Who is the listed applicant for Lunit INSIGHT MMG?

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

What is the FDA product code for Lunit INSIGHT MMG?

The FDA product code for Lunit INSIGHT MMG is QDQ.

Other records listing Lunit, 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.

K260320Lunit INSIGHT MMG (v1.1.10)K253796Lunit INSIGHT DBT (V1.2)K242652Lunit INSIGHT DBT v1.1K231470Lunit INSIGHT DBTK211733Lunit INSIGHT CXR Triage

Related Devices (Code: QDQ)

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.

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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.

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