The Multilift
FDA 510(k) K024346 · Services Industriels Savaria, Inc.
510(k) numberK024346
Submission
- Device name
- The Multilift
- Applicant
- Services Industriels Savaria, Inc.
Washington, DC, US - Received
- December 27, 2002
- Decision date
- March 4, 2003
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) summary available from FDA
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) | Device | Applicant | Decision |
|---|---|---|---|
| K113065 | RL, Ul, SL, El, and Epl Vertical Platform LiftsING · Traditional | Bella Elevator, LLC | 02/22/2012SE |
| K110495 | Liftkar PTING · Traditional | Sano Transportgerate GmbH | 05/20/2011SE |
| K102088 | Journey Inclined Platform Lift and Supra Curved Incline Platform LiftING · Special | Thyssenkrupp Ceteco Srl | 10/20/2010SE |
| K091881 | Rpl/Cpl Vertical Platform LiftsING · Traditional | Harmar Summit, LLC | 07/01/2009SE |
| K090856 | Journey (or RPSP), Journey Cubic (or Supra or TP02)ING · Traditional | Thyssenkrupp Ceteco Srl | 05/27/2009SE |
| K073513 | Merits E700 Porce LiftING · Abbreviated | Merits Health Products Co., Ltd. | 01/14/2008SE |
| K061514 | Bruno Vertical Platform Lift, Model VPL-3100ING · Traditional | Bruno Independent Living Aids, Inc. | 07/13/2006SE |
| K033469 | Genesis Vertical Platform LiftING · Abbreviated | Garaventa Accessibility | 01/07/2004SE |
| K020933 | Garaventa Super-Trac TRE-52ING · Special | Garaventa Accessibility | 04/04/2002SE |
| K983526 | Vertical LiftING · Traditional | Barnes,Richardson & Colburn | 12/11/1998SE |
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Questions and answers
When was The Multilift cleared by the FDA?
The Multilift (K024346) received a 510(k) decision of Substantially Equivalent on March 4, 2003, 67 days after the submission was received.
What is the product code of K024346?
The FDA product code is ING – Elevator, Wheelchair, Portable, a Class II (moderate risk) device regulated under 21 CFR 890.3930.