The objective of the study is to demonstrate that the FemPulse System can be used as indicated
The objective of the study is to demonstrate that the FemPulse System can be used as indicated in the Patient and Clinician Instructions for Use (IFU), as applicable.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
11
Subjects to receive the FemPulse System consisting of a non-implanted, vaginal electrical stimulation device (Ring) and other patient accessories.
Holy Cross Women's Hospital
Fort Lauderdale, Florida, United States
Patient Usability of System
A survery will be conducted to determine the overall usability of the system
Time frame: 2 days
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