Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR, NMPA) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

e-motion M25

K-Number: K221215 · 2022-05-24

ApplicantAlber GmbH
Decision Date2022-05-24
Product CodeITI
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

e-motion M25 is a medical device manufactured by Alber GmbH. It received FDA 510(k) clearance on 2022-05-24 under approval number K221215. The device is classified under product code ITI. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the e-motion M25?

e-motion M25 is a medical device that received FDA 510(k) clearance on 2022-05-24. It is manufactured by Alber GmbH. The 510(k) number is K221215.

When was e-motion M25 approved by the FDA?

e-motion M25 received FDA 510(k) clearance on 2022-05-24, under approval number K221215.

What company makes e-motion M25?

e-motion M25 is manufactured by Alber GmbH.

What is the FDA product code for e-motion M25?

The FDA product code for e-motion M25 is ITI.

Other Devices by Alber GmbH

K161241e-fix E35/E36 K151717twion K192618e-Motion M25 K192016SMOOV O10

Related Devices (Code: ITI)

K161241e-fix E35/E36Alber GmbH K153636Liberator Powered Wheelchair with Solar CompanionSolar Mobilityllc K160031Quickie Pulse (Models 6BC, 6SC, 6CC, 5BC, 5CC, 6MPC) and Zippie ZM-310 (Models BC, SC)Sunrise Medical (Us), LLC K151717twionAlber GmbH K153543WHILL Model MWhill, Inc. K152672Cajun Commando 4x4Lil Critter, LLC

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.

↑