Tilt Table 53
FDA 510(k) K841145 · S & W Enterprises, Inc.
510(k) numberK841145
Submission
- Device name
- Tilt Table 53
- Applicant
- S & W Enterprises, Inc.
Mchenry, IL, US - Received
- March 16, 1984
- Decision date
- April 13, 1984
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
Device classification
- Product code
- INQ – Table, Powered
- Device class
- Class I (low risk)
- Regulation
- 21 CFR 890.3760
- Specialty
- Physical Medicine
Other 510(k)s with product code INQ
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K960336 | Cardon Physical Therapy Table Model R27645INQ · Traditional | Cardon Rehabilitation Products, Inc. | 02/13/1996SE |
| K960334 | Cardon Physical Therapy Table Model R27116INQ · Traditional | Cardon Rehabilitation Products, Inc. | 02/13/1996SE |
| K960332 | Cardon Physical Therapy Table Model R28598INQ · Traditional | Cardon Rehabilitation Products, Inc. | 02/13/1996SE |
| K960196 | Tri W-G, Inc Table, Tilt/Exam/Treatment Model 777INQ · Traditional | Tri W-G, Inc. | 02/07/1996SE |
| K953621 | EVT-3300INQ · Traditional | U.S. Table, Inc. | 11/14/1995SE |
| K953622 | PTT 6200 Elevation Therapy TableINQ · Traditional | U.S. Table, Inc. | 09/11/1995SE |
| K952357 | The Hill Adjustable Podiatry ModelINQ · Traditional | Hill Laboratories Co. | 07/06/1995SE |
| K951419 | Flex D-4000INQ · Traditional | U.S. Table, Inc. | 06/30/1995SE |
| K952600 | EVT-5000BXINQ · Traditional | U.S. Table, Inc. | 06/22/1995SE |
| K952359 | The Hill Adjustable HA90CINQ · Traditional | Hill Laboratories Co. | 06/22/1995SE |
More from Hill Laboratories Co.
| 510(k) | Device | Decision |
|---|---|---|
| K864817 | S&W Model High-Low Mat Table, Various ModelsINQ · Traditional | 01/05/1987SE |
| K832768 | S & W SW52E W/Power Back LiftLGX · Traditional | 09/20/1983SE |
| K830873 | S & W Model AsoKNC · Traditional | 05/13/1983SE |
| K830875 | S & W Model 29JFB · Traditional | 04/08/1983SE |
| K830874 | S & W Model SW 37INQ · Traditional | 04/08/1983SE |
Questions and answers
When was Tilt Table 53 cleared by the FDA?
Tilt Table 53 (K841145) received a 510(k) decision of Substantially Equivalent on April 13, 1984, 28 days after the submission was received.
What is the product code of K841145?
The FDA product code is INQ – Table, Powered, a Class I (low risk) device regulated under 21 CFR 890.3760.