The following data is part of a premarket notification filed by Incontrol Medical, Llc with the FDA for Intonemv.
| Device ID | K133826 |
| 510k Number | K133826 |
| Device Name: | INTONEMV |
| Classification | Stimulator, Electrical, Non-implantable, For Incontinence |
| Applicant | INCONTROL MEDICAL, LLC 3225 GATEWAY ROAD, SUITE 250 Brookfield, WI 53045 |
| Contact | Jessica Andreshak |
| Correspondent | Jessica Andreshak INCONTROL MEDICAL, LLC 3225 GATEWAY ROAD, SUITE 250 Brookfield, WI 53045 |
| Product Code | KPI |
| CFR Regulation Number | 876.5320 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2013-12-17 |
| Decision Date | 2014-01-06 |
| Summary: | summary |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() INTONEMV 87952950 not registered Live/Pending |
InControl Medical, LLC 2018-06-07 |