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FDA 510(k)

DEKA Motus AY

K-Number: K181486 · 2018-08-30

ApplicantEl.En Electronic Engineering Spa
Decision Date2018-08-30
Product CodeGEX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

DEKA Motus AY 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 2018-08-30 under 510(k) number K181486. 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 AY?

DEKA Motus AY is a medical device that received FDA 510(k) clearance on 2018-08-30. The listed applicant is El.En Electronic Engineering Spa. The 510(k) number is K181486.

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

DEKA Motus AY received FDA 510(k) clearance on 2018-08-30, under 510(k) number K181486.

Who is the listed applicant for DEKA Motus AY?

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 AY?

The FDA product code for DEKA Motus AY 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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