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FDA 510(k)

DEKA Motus AZ

K-Number: K211821 · 2021-07-06

ApplicantEl.En Electronic Engineering Spa
Decision Date2021-07-06
Product CodeGEX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

DEKA Motus AZ is the device name listed in this FDA 510(k) record. The listed applicant is El.En Electronic Engineering Spa. It received FDA 510(k) clearance on 2021-07-06 under 510(k) number K211821. 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 DEKA Motus AZ?

DEKA Motus AZ is a medical device that received FDA 510(k) clearance on 2021-07-06. The listed applicant is El.En Electronic Engineering Spa. The 510(k) number is K211821.

When did DEKA Motus AZ receive FDA 510(k) clearance?

DEKA Motus AZ received FDA 510(k) clearance on 2021-07-06, under 510(k) number K211821.

Who is the listed applicant for DEKA Motus AZ?

The FDA 510(k) record lists El.En Electronic Engineering Spa as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DEKA Motus AZ?

The FDA product code for DEKA Motus AZ is GEX. This falls under the Gastroenterology category.

Other records listing El.En Electronic Engineering Spa as applicant

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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.

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