FDA product code INQ: Table, Powered
INQ is the FDA product code for table, powered. It is a Class I device, regulated under 21 CFR 890.3760 and reviewed by the Physical Medicine panel. FDA has cleared 102 510(k) submissions under INQ, from 35 different applicants. The average 510(k) review took 80 days (median 56). FDA has posted 2 recalls for INQ devices.
Classification
| Field | Value |
|---|---|
| Device name | Table, Powered |
| Device class | Class I |
| Regulation | 21 CFR 890.3760 |
| Review panel | PM — Physical Medicine |
| Medical specialty | Physical Medicine |
| Premarket route | 510(k) exempt |
Compare with all 510(k) review times · Search every INQ clearance
Top INQ applicants
| Applicant | Clearances | Latest |
|---|---|---|
| Cardon Rehabilitation Products, Inc. | 16 | 1996-02-13 |
| Tri W-G, Inc. | 14 | 1996-02-07 |
| Hill Laboratories Co. | 10 | 1995-07-06 |
| Bailey Mfg. Co. | 6 | 1993-07-22 |
| Midland Mfg. Co. | 6 | 1993-03-24 |
30 more applicants have INQ clearances. See the full list in Caduvo.
Most recent INQ clearances
| 510(k) | Applicant | Device | Decision date | Review days |
|---|---|---|---|---|
| K960334 | Cardon Rehabilitation Products, Inc. | CARDON PHYSICAL THERAPY TABLE MODEL R27116 | 1996-02-13 | 20 |
| K960336 | Cardon Rehabilitation Products, Inc. | CARDON PHYSICAL THERAPY TABLE MODEL R27645 | 1996-02-13 | 20 |
| K960332 | Cardon Rehabilitation Products, Inc. | CARDON PHYSICAL THERAPY TABLE MODEL R28598 | 1996-02-13 | 20 |
| K960196 | Tri W-G, Inc. | TRI W-G, INC TABLE, TILT/EXAM/TREATMENT MODEL 777 | 1996-02-07 | 22 |
| K953621 | U.S. Table, Inc. | EVT-3300 | 1995-11-14 | 103 |
Recalls for INQ devices
2 product recalls in 2 recall events; 0 initiated in the last five years and 0 still open. Most recent: 2016-06-29.
Frequently asked questions
What is FDA product code INQ?
INQ is the FDA product code for table, powered. It is a Class I device, regulated under 21 CFR 890.3760 and reviewed by the Physical Medicine panel.
What device class is INQ?
Class I, regulation 21 CFR 890.3760. Typical premarket route: 510(k) exempt.
How long does a 510(k) take for product code INQ?
Across 102 cleared submissions the average was 80 days from receipt to decision (median 56).
Which companies have the most INQ clearances?
Cardon Rehabilitation Products, Inc. (16); Tri W-G, Inc. (14); Hill Laboratories Co. (10); Bailey Mfg. Co. (6); Midland Mfg. Co. (6).
Have INQ devices been recalled?
Yes: 2 product recalls across 2 recall events; the most recent began 2016-06-29.
Next steps
- Run an FDA pathway report with predicate devices for product code INQ
- Run a recall and safety report across every INQ manufacturer
- Watch product code INQ 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.
All Physical Medicine product codes · FDA product code lookup · 510(k) database search · 510(k) review times