FDA product code ING: Elevator, Wheelchair, Portable
ING is the FDA product code for elevator, wheelchair, portable. It is a Class II device, regulated under 21 CFR 890.3930 and reviewed by the Physical Medicine panel. FDA has cleared 29 510(k) submissions under ING, from 19 different applicants. The average 510(k) review took 63 days (median 58). FDA has posted 3 recalls for ING devices.
Definition
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).
Classification
| Field | Value |
|---|---|
| Device name | Elevator, Wheelchair, Portable |
| Device class | Class II |
| Regulation | 21 CFR 890.3930 |
| Review panel | PM — Physical Medicine |
| Medical specialty | Physical Medicine |
| Premarket route | 510(k) |
| Third-party 510(k) review eligible | Yes |
Compare with all 510(k) review times · Search every ING clearance
Top ING applicants
| Applicant | Clearances | Latest |
|---|---|---|
| Crow River Industries, Inc. | 4 | 1995-11-29 |
| The Cheney Co. | 3 | 1990-01-12 |
| Thyssenkrupp Ceteco Srl | 2 | 2010-10-20 |
| Garaventa Accessibility | 2 | 2004-01-07 |
| Services Industriels Savaria, Inc. | 2 | 2003-03-04 |
14 more applicants have ING clearances. See the full list in Caduvo.
Most recent ING clearances
| 510(k) | Applicant | Device | Decision date | Review days |
|---|---|---|---|---|
| K113065 | Bella Elevator, LLC | RL, UL, SL, EL, AND EPL VERTICAL PLATFORM LIFTS | 2012-02-22 | 131 |
| K110495 | Sano Transportgerate GmbH | LIFTKAR PT | 2011-05-20 | 87 |
| K102088 | Thyssenkrupp Ceteco Srl | JOURNEY INCLINED PLATFORM LIFT AND SUPRA CURVED INCLINE PLATFORM LIFT | 2010-10-20 | 86 |
| K091881 | Harmar Summit, LLC | RPL/CPL VERTICAL PLATFORM LIFTS | 2009-07-01 | 7 |
| K090856 | Thyssenkrupp Ceteco Srl | JOURNEY (OR RPSP), JOURNEY CUBIC (OR SUPRA OR TP02) | 2009-05-27 | 58 |
Recalls for ING devices
3 product recalls in 1 recall events; 0 initiated in the last five years and 0 still open. Most recent: 2007-08-15.
Frequently asked questions
What is FDA product code ING?
ING is the FDA product code for elevator, wheelchair, portable. It is a Class II device, regulated under 21 CFR 890.3930 and reviewed by the Physical Medicine panel.
What device class is ING?
Class II, regulation 21 CFR 890.3930. Typical premarket route: 510(k).
How long does a 510(k) take for product code ING?
Across 29 cleared submissions the average was 63 days from receipt to decision (median 58).
Which companies have the most ING clearances?
Crow River Industries, Inc. (4); The Cheney Co. (3); Thyssenkrupp Ceteco Srl (2); Garaventa Accessibility (2); Services Industriels Savaria, Inc. (2).
Have ING devices been recalled?
Yes: 3 product recalls across 1 recall events; the most recent began 2007-08-15.
Next steps
- Run an FDA pathway report with predicate devices for product code ING
- Run a recall and safety report across every ING manufacturer
- Watch product code ING for new clearances and recalls
Source: openFDA device classification, 510(k), PMA, De Novo and recall data (public domain). Review days run from FDA receipt to decision. Not regulatory advice.
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