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 |