Xltek Protektor Stimulator, Models 10247 & 10248
FDA 510(k) K040358 · Excel Tech. , Ltd.
510(k) numberK040358
Submission
- Device name
- Xltek Protektor Stimulator, Models 10247 & 10248
- Applicant
- Excel Tech. , Ltd.
Oakville, Ontario, CA - Received
- February 13, 2004
- Decision date
- August 6, 2004
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) statement available from FDA
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| K062549 | Xltek Stimulator Probes, Models 105233, 105234, 105235, 105236, 105237 and 105238ETN · Traditional | 10/04/2006SE |
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| K053058 | Xltek Neuropath, Model PK1070JXE · Traditional | 02/07/2006SE |
| K052112 | Xltek Xcalibur Emg / LT, Model PK1P33, PK1059IKN · Special | 10/28/2005SE |
| K052111 | Xltek Clear Signal Sub-Dermal Needle, Models 102889, 102798, 102799, 102382GXZ · Abbreviated | 08/17/2005SE |
| K042223 | Xltek Connex Ip Headbox, Model 1054OMB · Special | 09/16/2004SE |
| K042150 | Xltek Trex MODEL#10309GWQ · Special | 08/27/2004SE |
| K040360 | EMU128S, Model EX-NW-128SGWQ · Special | 03/12/2004SE |
| K022037 | Xltek Sleep SystemOLV · Special | 09/10/2002SE |
Questions and answers
When was Xltek Protektor Stimulator, Models 10247 & 10248 cleared by the FDA?
Xltek Protektor Stimulator, Models 10247 & 10248 (K040358) received a 510(k) decision of Substantially Equivalent on August 6, 2004, 175 days after the submission was received.
What is the product code of K040358?
The FDA product code is GWF – Stimulator, Electrical, Evoked Response, a Class II (moderate risk) device regulated under 21 CFR 882.1870.