UROSTYM BIOFEEDBACK AND STIMULATION DEVICE AND ACCESSORIES— 510(k) K070331
Substantially EquivalentLaborie Medical Technologies
FDA 510(k) clearance K070331 for UROSTYM BIOFEEDBACK AND STIMULATION DEVICE AND ACCESSORIES, Substantially Equivalent on 2007-05-04. Applicant: Laborie Medical Technologies. Device class: 2.
Clearance details
- Applicant
- Laborie Medical Technologies
- Product code
- Code KPI
- Device class
- Class 2
- Regulation
- 21 CFR 876.5320
- Advisory panel
- Gastroenterology, Urology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Williston, VT, US
Recent devices under product code KPI
view all- K260178 — Pelvic Muscle Trainer (KM510, KM516B)
- K252601 — Pelvic Muscle Trainer (4 models)
- K252552 — Pelvic Floor Rehabilitation Therapy Device (PD2301/PD2302/PD2303)
- K252831 — Pelvic Floor Treatment Device (DLR-8920, DLR-8921, DLR-8922, DLR-8923, DLR-8924, DLR-8925, DLR-8926, DLR-8927)
- K252334 — PELVIPOWER Pelvic Functional Magnetic Stimulation (PELVIPOWER PelvicFMS) (033-0-1100-02)
Data sourced from openFDA. This site is unofficial and independent of the FDA.