The following data is part of a premarket notification filed by Btl Industries, Inc. with the FDA for Hpm-6000uf.
Device ID | K181497 |
510k Number | K181497 |
Device Name: | HPM-6000UF |
Classification | Stimulator, Electrical, Non-implantable, For Incontinence |
Applicant | BTL Industries, Inc. 362 Elm Street Marlborough, MA 01752 |
Contact | David Chmel |
Correspondent | David Chmel BTL Industries, Inc. 362 Elm Street Marlborough, MA 01752 |
Product Code | KPI |
CFR Regulation Number | 876.5320 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2018-06-07 |
Decision Date | 2018-11-14 |
Summary: | summary |