Powermatic Treatment Table
FDA 510(k) K933581 · Medical Device Inspection Co., Inc.
510(k) numberK933581
Submission
- Device name
- Powermatic Treatment Table
- Applicant
- Medical Device Inspection Co., Inc.
Great Neck, NY, US - Received
- July 22, 1993
- Decision date
- November 5, 1993
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) statement available from FDA
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 |
|---|---|---|
| K945826 | J & J I-330 Series Physiological Monitoring & Biofeedback Instument and Use Software…HCC · Traditional | 08/04/1995SE |
| K932072 | Jarit Surgical InstrumentsHET · Traditional | 01/11/1994SE |
| K931594 | Thera-Turn CM-1000 Mattress Overlay SystemIOQ · Traditional | 12/21/1993SE |
| K933580 | Power Work TableINQ · Traditional | 11/05/1993SE |
| K933578 | Powermatic Mat PlatformINQ · Traditional | 11/05/1993SE |
| K933577 | Powermatic Examination TableINQ · Traditional | 09/30/1993SE |
| K922045 | Shower ChairsINM · Traditional | 05/26/1992SE |
| K912075 | C-Section TrayKNA · Traditional | 04/07/1992SESK |
| K914174 | Sterile Disposable Wet Skin Scrub TrayLRO · Traditional | 02/24/1992SEKD |
| K920403 | Xenon Arc Endoscope Light SourceGCJ · Traditional | 02/21/1992SE |
Questions and answers
When was Powermatic Treatment Table cleared by the FDA?
Powermatic Treatment Table (K933581) received a 510(k) decision of Substantially Equivalent on November 5, 1993, 106 days after the submission was received.
What is the product code of K933581?
The FDA product code is INQ – Table, Powered, a Class I (low risk) device regulated under 21 CFR 890.3760.