Neuroline, Disposable Concentric Needle Electrodes
FDA 510(k) K973529 · Medicotest A/S
510(k) numberK973529
Submission
- Device name
- Neuroline, Disposable Concentric Needle Electrodes
- Applicant
- Medicotest A/S
Washington, DC, US - Received
- September 18, 1997
- Decision date
- November 20, 1997
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) statement available from FDA
Device classification
- Product code
- IKT – Electrode, Needle, Diagnostic Electromyograph
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 890.1385
- Specialty
- Physical Medicine
Other 510(k)s with product code IKT
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K253581 | Disposable Concentric Needle Electrode 0.30x25mm Red (TE/B50700-001); Disposable…IKT · Traditional | Technomed Europe | 03/15/2026SE |
| K173815 | Allergan Botox Needle ElectrodeIKT · Traditional | Natus Manufacturing Limited | 06/29/2018SE |
| K161430 | Myoject Luer Lock Needle ElectrodeIKT · Traditional | Natus Manufacturing Limited | 03/02/2017SE |
| K152984 | Disposable Concentric Needle electrodes, Disposable Monopolar Needle electrodes…IKT · Traditional | Bio Protech, Inc. | 06/03/2016SE |
| K143433 | Dantec DCN Disposable Concentric Needle Electrodes-25mm, Dantec DCN Disposable…IKT · Traditional | Natus Manufacturing Limited | 08/28/2015SE |
| K120342 | Emg Recording Electrode AssemblyIKT · Traditional | Rhythmlink International, LLC | 06/22/2012SE |
| K112034 | Teca Elite Disposable Concentric NeedlesIKT · Special | Carefusion 209, Inc. | 08/12/2011SE |
| K111131 | Teca (TM) Elite Disposable Monopolar NeedlesIKT · Special | Carefusion 209, Inc. | 06/17/2011SE |
| K092973 | Disposable and Reusable Concentric Needles / Disposable and Reusable Monopolar NeedleIKT · Traditional | Bionen S.A.S. | 10/07/2010SE |
| K093825 | Ambu Neuroline Disposable Inoject Needle ElectrodeIKT · Special | Ambu A/S | 01/13/2010SE |
More from Ambu A/S
| 510(k) | Device | Decision |
|---|---|---|
| K020382 | Blue Sensor, Disposable ECG Electrodes for AnaesthesiaDRX · Traditional | 06/28/2002SE |
| K020907 | Neuroline, Subdermal Needle ElectrodesIKT · Traditional | 06/14/2002SE |
| K002079 | Multi-Function Defibrillation ElectrodeMKJ · Traditional | 02/22/2001SE |
| K001869 | Diagnostic Electromyography Needle Electrode, Disposable Hypodermic NeedleIKT · Traditional | 09/18/2000SE |
| K983689 | Blue Sensor Supatab,Disposable ECG ElectrodesDRX · Traditional | 01/15/1999SE |
| K965194 | Medicom, TENS ElectrodesGXY · Traditional | 03/06/1997SE |
Questions and answers
When was Neuroline, Disposable Concentric Needle Electrodes cleared by the FDA?
Neuroline, Disposable Concentric Needle Electrodes (K973529) received a 510(k) decision of Substantially Equivalent on November 20, 1997, 63 days after the submission was received.
What is the product code of K973529?
The FDA product code is IKT – Electrode, Needle, Diagnostic Electromyograph, a Class II (moderate risk) device regulated under 21 CFR 890.1385.