FDA 510(k)
FDA class 2
Unknown
🇺🇸 United States
Quell-FM
K Number: DEN210046
·
Decision May 18, 2022
Classifications
1
FEI Numbers
1
Registration Numbers
1
Same Product Code
0
Applicant Total
18
Review Days
225
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Basic Information
- Device Name
- Quell-FM
- K Number
- DEN210046
- Device Class
- FDA class 2
- Clearance Type
- Direct
- Regulation Number
- 882.5888
- Medical Specialty
- Neurology
- Decision
- Unknown
- Applicant
- Neurometrix, Inc.
- Date Received
- October 5, 2021
- Decision Date
- May 18, 2022
- Product Code
- QSQ
- Advisory Committee
- Neurology
- Review Advisory Committee
- NE
- Third Party
- N
Classifications
This FDA 510(k) entry is associated with 1 FDA classification via its product code.
| Product Code | Device Name | Device Class | Medical Specialty |
|---|---|---|---|
| QSQ | Transcutaneous Electrical Nerve Stimulator To Treat Fibromyalgia Symptoms | FDA class 2 | Neurology |
Other Clearances by Neurometrix, Inc.
| K Number | Device Name | ||
|---|---|---|---|
| K152954 | Quell | Jan 5, 2016 | Substantially Equivalent |
| K140586 | ASCEND ELECTRODE | Nov 17, 2014 | Substantially Equivalent |
| K140333 | ASCEND | Jul 3, 2014 | Substantially Equivalent |
| K130919 | SENSUS | Jul 2, 2013 | Substantially Equivalent |
| K121816 | SENSUS ELECTRODE | Nov 26, 2012 | Substantially Equivalent |
| K121184 | SENSUS | Aug 2, 2012 | Substantially Equivalent |
| K091155 | ASCEND | Sep 3, 2009 | Substantially Equivalent |
| K083322 | NEUROMETRIX BIOAMPLIFIER | May 27, 2009 | Substantially Equivalent |
| K083818 | UNIVERSAL ELECTRODES | Jan 21, 2009 | Substantially Equivalent |
| K081871 | UNIVERSAL ELECTRODES | Sep 29, 2008 | Substantially Equivalent |