510(k) K151922
K151922 is an FDA 510(k) premarket notification submitted by Stimmed, LLC for the device "StimSox(TM) System". The FDA issued a decision of Substantially Equivalent on Apr 15, 2016. The device falls under product code IPF (Stimulator, Muscle, Powered), a Class II device regulated under 21 CFR 890.5850. Stimmed, LLC has 1 other 510(k) clearance on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Apr 15, 2016
- Date Received
- Jul 13, 2015
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Stimulator, Muscle, Powered
- Device Class
- Class II
- Regulation Number
- 890.5850
- Review Panel
- PM
- Submission Type
- 510(k)