Table, Models 610,611 & 612
FDA 510(k) K834103 · Tri W-G, Inc.
510(k) numberK834103
Submission
- Device name
- Table, Models 610,611 & 612
- Applicant
- Tri W-G, Inc.
Mchenry, IL, US - Received
- November 29, 1983
- Decision date
- January 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 |
|---|---|---|
| K960196 | Tri W-G, Inc Table, Tilt/Exam/Treatment Model 777INQ · Traditional | 02/07/1996SE |
| K945163 | EchocardiographyLGX · Traditional | 02/17/1995SE |
| K941720 | Model 747 and 747-30 Exam/Treatment TableINQ · Traditional | 05/06/1994SE |
| K936303 | Treatment Table ModificationINQ · Traditional | 03/18/1994SE |
| K933119 | Hi-Lo Treatment TablesINQ · Traditional | 10/12/1993SE |
| K932746 | Model T4501,T4502,T4503,T4504,T4504 Tilt TableINQ · Traditional | 07/21/1993SE |
| K930802 | Models 642 & 643 Tilt Exam/Treatment TableINQ · Traditional | 03/22/1993SE |
| K925594 | MDL 29001 Medi Elec-Mech Tilt Exam/Treatment TableINQ · Traditional | 02/12/1993SE |
| K923325 | Model 600 Medical Treatment TableINQ · Traditional | 07/21/1992SE |
| K922980 | 745-M (Magnum)JFB · Traditional | 07/13/1992SE |
Questions and answers
When was Table, Models 610,611 & 612 cleared by the FDA?
Table, Models 610,611 & 612 (K834103) received a 510(k) decision of Substantially Equivalent on January 13, 1984, 45 days after the submission was received.
What is the product code of K834103?
The FDA product code is INQ – Table, Powered, a Class I (low risk) device regulated under 21 CFR 890.3760.