Inclinometer
FDA 510(k) K954647 · J-Tech, Inc.
510(k) numberK954647
Submission
- Device name
- Inclinometer
- Applicant
- J-Tech, Inc.
Alpine, UT, US - Received
- October 10, 1995
- Decision date
- October 30, 1995
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) summary available from FDA
Device classification
- Product code
- KQX – Goniometer, Ac-Powered
- Device class
- Class I (low risk)
- Regulation
- 21 CFR 888.1500
- Specialty
- Orthopedic
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|---|---|---|---|
| K011827 | Ortelius 800KQX · Traditional | Orthoscan , Ltd. | 08/28/2001SE |
| K971079 | Interlogics W-Tracker and Wrist Works SoftwareKQX · Traditional | Interlogics, Inc. | 07/09/1997SE |
| K962377 | 3D-SPINEKQX · Traditional | Skill Technologies, Inc. | 09/03/1996SE |
| K961212 | Spinal TouchKQX · Traditional | Fasstech | 06/12/1996SE |
| K943929 | Dataglove and Movement Analysis System (Mas)KQX · Traditional | Greenleaf Medical Systems, Inc. | 05/15/1995SE |
| K945630 | Large Muscle Strength GaugeKQX · Traditional | J-Tech, Inc. | 05/10/1995SE |
| K943898 | Saunders Electronic InclinometerKQX · Traditional | The Saunders Group | 11/28/1994SE |
| K940812 | Insight Electronic Alignment IndicatorKQX · Traditional | Andronic Devices, Ltd. | 11/21/1994SE |
| K925225 | The Bte Vector; Analysis System for the Low BackKQX · Traditional | Baltimore Therapeutic Equipment Co. | 06/27/1994SE |
| K933063 | Isotechnologies Back Tracker and Back Works SoftwaKQX · Traditional | Isotechnologies, Inc. | 01/27/1994SE |
More from Isotechnologies, Inc.
| 510(k) | Device | Decision |
|---|---|---|
| K954737 | Surface Electromyograph Biofeedback Muscle Activity DeviceHCC · Traditional | 07/03/1996SE |
| K945630 | Large Muscle Strength GaugeKQX · Traditional | 05/10/1995SE |
| K913587 | Jtech 50 Series Cutting LoopFJL · Traditional | 10/23/1991SE |
| K912526 | GS-220 Hand Impairment Evaluation SystemLBB · Traditional | 09/05/1991SE |
Questions and answers
When was Inclinometer cleared by the FDA?
Inclinometer (K954647) received a 510(k) decision of Substantially Equivalent on October 30, 1995, 20 days after the submission was received.
What is the product code of K954647?
The FDA product code is KQX – Goniometer, Ac-Powered, a Class I (low risk) device regulated under 21 CFR 888.1500.