Easy Life

FDA 510(k) K023521 · Berkline Corp.

Substantially Equivalent

510(k) numberK023521

Submission

Device name
Easy Life
Applicant
Berkline Corp.
Morristown, TN, US
Received
October 21, 2002
Decision date
November 19, 2002
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
INO – Chair, Positioning, Electric
Device class
Class II (moderate risk)
Regulation
21 CFR 890.3110
Specialty
Physical Medicine

Other 510(k)s with product code INO

510(k)DeviceApplicantDecision
K131909Dalton Lift ChairINO · Traditional Dalton Instrument Corp.02/24/2014SE
K123834Easystand Bantam MediumINO · Traditional Altimate Medical, Inc.08/13/2013SE
K112944Fresenius Medical Treatment Chair T688 SeriesINO · Traditional Fresenius Medical Care South Asia Pacific Pty…12/30/2011SE
K101723Compact Wheelchair PlatformINO · Traditional Design Specific Fletcher12/23/2010SE
K091578Lift Chair, Model T3INO · Special Pride Mobility Products Corp.12/02/2009SE
K091727Medical Treatment Chair, T400, T500,T600INO · Traditional Fresenius Medical Care South Asia Pacific Pty…07/06/2009SE
K091242BantamINO · Traditional Altimate Medical, Inc.07/06/2009SE
K073565Standard Wheelchair PlatformINO · Traditional Design Specific , Ltd.02/06/2009SE
K081053Pivot AssistINO · Traditional Pivot Assist, LLC10/09/2008SE
K080533Winco Model Power Series Lift ChairINO · Traditional Winco, Inc.08/11/2008SE

Questions and answers

When was Easy Life cleared by the FDA?

Easy Life (K023521) received a 510(k) decision of Substantially Equivalent on November 19, 2002, 29 days after the submission was received.

What is the product code of K023521?

The FDA product code is INO – Chair, Positioning, Electric, a Class II (moderate risk) device regulated under 21 CFR 890.3110.