Goniometer and Biomedical Recorder System
FDA 510(k) K884003 · Penny & Giles Blackwood , Ltd.
510(k) numberK884003
Submission
- Device name
- Goniometer and Biomedical Recorder System
- Applicant
- Penny & Giles Blackwood , Ltd.
England, GB - Received
- September 21, 1988
- Decision date
- December 19, 1988
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
Device classification
- Product code
- KQX – Goniometer, Ac-Powered
- Device class
- Class I (low risk)
- Regulation
- 21 CFR 888.1500
- Specialty
- Orthopedic
Other 510(k)s with product code KQX
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| 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 |
| K954647 | InclinometerKQX · Traditional | J-Tech, Inc. | 10/30/1995SE |
| 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 |
Questions and answers
When was Goniometer and Biomedical Recorder System cleared by the FDA?
Goniometer and Biomedical Recorder System (K884003) received a 510(k) decision of Substantially Equivalent on December 19, 1988, 89 days after the submission was received.
What is the product code of K884003?
The FDA product code is KQX – Goniometer, Ac-Powered, a Class I (low risk) device regulated under 21 CFR 888.1500.