FDA product code IQB: Belt, Wheelchair
IQB is the FDA product code for belt, wheelchair. It is a Class I device, regulated under 21 CFR 890.3920 and reviewed by the Physical Medicine panel. FDA has cleared 2 510(k) submissions under IQB. The average 510(k) review took 9 days (median 9).
Classification
| Field | Value |
|---|---|
| Device name | Belt, Wheelchair |
| Device class | Class I |
| Regulation | 21 CFR 890.3920 |
| Review panel | PM — Physical Medicine |
| Medical specialty | Physical Medicine |
| Premarket route | 510(k) exempt |
Compare with all 510(k) review times · Search every IQB clearance
Top IQB applicants
| Applicant | Clearances | Latest |
|---|---|---|
| Fred Sammons, Inc. | 2 | 1978-01-05 |
Most recent IQB clearances
| 510(k) | Applicant | Device | Decision date | Review days |
|---|---|---|---|---|
| K772420 | Fred Sammons, Inc. | REAR FASTENING SAFETY STRAP | 1978-01-05 | 9 |
| K772421 | Fred Sammons, Inc. | WHEELCHAIR BELT | 1978-01-05 | 9 |
Recalls for IQB devices
openFDA lists no recalls for product code IQB.
Frequently asked questions
What is FDA product code IQB?
IQB is the FDA product code for belt, wheelchair. It is a Class I device, regulated under 21 CFR 890.3920 and reviewed by the Physical Medicine panel.
What device class is IQB?
Class I, regulation 21 CFR 890.3920. Typical premarket route: 510(k) exempt.
How long does a 510(k) take for product code IQB?
Across 2 cleared submissions the average was 9 days from receipt to decision (median 9).
Which companies have the most IQB clearances?
Fred Sammons, Inc. (2).
Next steps
- Run an FDA pathway report with predicate devices for product code IQB
- Run a recall and safety report across every IQB manufacturer
- Watch product code IQB 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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