510(k) K150183
K150183 is an FDA 510(k) premarket notification submitted by Incontrol Medical, LLC for the device "ApexM". The FDA issued a decision of Substantially Equivalent on Apr 9, 2015. The device falls under product code KPI (Stimulator, Electrical, Non-Implantable, For Incontinence), a Class II device regulated under 21 CFR 876.5320. Incontrol Medical, LLC has 6 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Apr 9, 2015
- Date Received
- Jan 27, 2015
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Stimulator, Electrical, Non-Implantable, For Incontinence
- Device Class
- Class II
- Regulation Number
- 876.5320
- Review Panel
- GU
- Submission Type
- 510(k)