510(k) K131159
K131159 is an FDA 510(k) premarket notification submitted by Chattem, Inc. for the device "SMARTRELIEF". The FDA issued a decision of Substantially Equivalent on Jul 25, 2013. The device falls under product code NUH (Stimulator, Nerve, Transcutaneous, Over-The-Counter), a Class II device regulated under 21 CFR 882.5890.
Clearance details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Jul 25, 2013
- Date Received
- Apr 24, 2013
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device classification
- Device Name
- Stimulator, Nerve, Transcutaneous, Over-The-Counter
- Device Class
- Class II
- Regulation Number
- 882.5890
- Review Panel
- NE
- Submission Type
- 510(k)
TEMPORARY RELIEF OF PAIN DUE TO SORE/ACHING MUSCLES