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FDA 510(k)

Darwin

K-Number: K203728 · 2021-07-14

ApplicantLuvo Medical Technologies, Inc.
Decision Date2021-07-14
Product CodeGEX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

Darwin is the device name listed in this FDA 510(k) record. The listed applicant is Luvo Medical Technologies, Inc.. It received FDA 510(k) clearance on 2021-07-14 under 510(k) number K203728. The device is classified under product code GEX. It was reviewed by the SU advisory panel. Product code GEX falls under the category of Gastroenterology, which includes gastrointestinal diagnostic and therapeutic devices. Devices in this category are subject to specific FDA regulatory requirements. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Darwin?

Darwin is a medical device that received FDA 510(k) clearance on 2021-07-14. The listed applicant is Luvo Medical Technologies, Inc.. The 510(k) number is K203728.

When did Darwin receive FDA 510(k) clearance?

Darwin received FDA 510(k) clearance on 2021-07-14, under 510(k) number K203728.

Who is the listed applicant for Darwin?

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

What is the FDA product code for Darwin?

The FDA product code for Darwin is GEX. This falls under the Gastroenterology category.

Other records listing Luvo Medical Technologies, 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.

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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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