Genesis Vertical Platform Lift

FDA 510(k) K033469 · Garaventa Accessibility

Substantially Equivalent

510(k) numberK033469

Submission

Device name
Genesis Vertical Platform Lift
Applicant
Garaventa Accessibility
Surrey, British Columbia, CA
Received
November 3, 2003
Decision date
January 7, 2004
Decision
Substantially Equivalent (SESE)
Type
Abbreviated 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
ING – Elevator, Wheelchair, Portable
Device class
Class II (moderate risk)
Regulation
21 CFR 890.3930
Specialty
Physical Medicine

A motorized lift device that is not permanently mounted in one location and that is intended for medical purposes to provide a means to move a person with impaired mobility, with or without a wheelchair, from one level to another (e.g., portable platform lifts, attendant-operated stair climbing devices for wheelchairs).

Other 510(k)s with product code ING

510(k)DeviceApplicantDecision
K113065RL, Ul, SL, El, and Epl Vertical Platform LiftsING · Traditional Bella Elevator, LLC02/22/2012SE
K110495Liftkar PTING · Traditional Sano Transportgerate GmbH05/20/2011SE
K102088Journey Inclined Platform Lift and Supra Curved Incline Platform LiftING · Special Thyssenkrupp Ceteco Srl10/20/2010SE
K091881Rpl/Cpl Vertical Platform LiftsING · Traditional Harmar Summit, LLC07/01/2009SE
K090856Journey (or RPSP), Journey Cubic (or Supra or TP02)ING · Traditional Thyssenkrupp Ceteco Srl05/27/2009SE
K073513Merits E700 Porce LiftING · Abbreviated Merits Health Products Co., Ltd.01/14/2008SE
K061514Bruno Vertical Platform Lift, Model VPL-3100ING · Traditional Bruno Independent Living Aids, Inc.07/13/2006SE
K024346The MultiliftING · Traditional Services Industriels Savaria, Inc.03/04/2003SE
K020933Garaventa Super-Trac TRE-52ING · Special Garaventa Accessibility04/04/2002SE
K983526Vertical LiftING · Traditional Barnes,Richardson & Colburn12/11/1998SE

More from Barnes,Richardson & Colburn

510(k)DeviceDecision
K020933Garaventa Super-Trac TRE-52ING · Special 04/04/2002SE

Questions and answers

When was Genesis Vertical Platform Lift cleared by the FDA?

Genesis Vertical Platform Lift (K033469) received a 510(k) decision of Substantially Equivalent on January 7, 2004, 65 days after the submission was received.

What is the product code of K033469?

The FDA product code is ING – Elevator, Wheelchair, Portable, a Class II (moderate risk) device regulated under 21 CFR 890.3930.