Liberty
FDA 510(k) K943250 · Utah Medical Products, Inc.
510(k) numberK943250
Submission
- Device name
- Liberty
- Applicant
- Utah Medical Products, Inc.
Midvale, UT, US - Received
- July 6, 1994
- Decision date
- February 9, 1995
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) summary available from FDA
Device classification
- Product code
- KPI – Stimulator, Electrical, Non-Implantable, For Incontinence
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 876.5320
- Specialty
- Gastroenterology, Urology
Other 510(k)s with product code KPI
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K260178 | Pelvic Muscle Trainer (KM510, KM516B)KPI · Traditional | Shenzhen Konmed Technology Co., Ltd. | 06/18/2026SE |
| K252601 | Pelvic Muscle Trainer (PC22A); Pelvic Muscle Trainer (PC22A-L); Pelvic Muscle Trainer…KPI · Traditional | Hunan Accurate Bio-Medical Technology Co., Ltd. | 05/14/2026SE |
| K252552 | Pelvic Floor Rehabilitation Therapy Device (PD2301/PD2302/PD2303)KPI · Traditional | Shenzhen Changkun Technology Co., Ltd. | 05/06/2026SE |
| K252831 | Pelvic Floor Treatment Device (DLR-8920, DLR-8921, DLR-8922, DLR-8923, DLR-8924…KPI · Traditional | Dolanvy (Suzhou) Medical Technology Co., Ltd. | 04/28/2026SE |
| K252334 | PELVIPOWER Pelvic Functional Magnetic Stimulation (PELVIPOWER PelvicFMS) (033-0-1100-02)KPI · Traditional | Pontemedag | 04/17/2026SE |
| K251760 | Well-Life Incontinence Stimulation System (WL-2405i(P))KPI · Traditional | Well-Life Healthcare , Ltd. | 02/12/2026SE |
| K251026 | Regenesis EMS ChairKPI · Traditional | Trinity Medical Solutions | 08/29/2025SE |
| K243079 | NeuroTrac® MyoPlus Pro (MYO120U)KPI · Traditional | Verity Medical , Ltd. | 06/26/2025SE |
| K241862 | Levina Pelvic Floor Muscle Stimulator (RS-48)KPI · Traditional | Zmi Electronics , Ltd. | 03/27/2025SE |
| K241516 | BTL-398KPI · Traditional | BTL Industries, Inc. | 02/10/2025SE |
More from BTL Industries, Inc.
| 510(k) | Device | Decision |
|---|---|---|
| K143424 | Utah Cvx-RipePFJ · Traditional | 08/28/2015SE |
| K123310 | Finesse 3RD Generation (Models Finesse+ and Finesseii+)GEI · Traditional | 01/23/2013SE |
| K101535 | Bt-CathOQY · Traditional | 01/11/2011SE |
| K063611 | Saline/ Contrast Media Infusion CatheterLKF · Traditional | 05/23/2007SE |
| K001874 | Peripherally Inserted Central CatheterLJS · Traditional | 09/25/2000SE |
| K000974 | Fowler Endocurette, Model Cur-XxxHHK · Traditional | 05/23/2000SE |
| K965245 | TBDHGI · Traditional | 07/03/1997SE |
| K970077 | Liberty Plus SYSTEM(PFS-300)/VAGINAL Probe, Liberty PLUS(PFS-044)KPI · Traditional | 05/23/1997SE |
| K955663 | Abc In-Line Blood Sampling KitCBT · Traditional | 03/17/1997SE |
| K964526 | Liberty Rectal Pelvic Floor ExerciserKPI · Traditional | 02/10/1997SE |
Questions and answers
When was Liberty cleared by the FDA?
Liberty (K943250) received a 510(k) decision of Substantially Equivalent on February 9, 1995, 218 days after the submission was received.
What is the product code of K943250?
The FDA product code is KPI – Stimulator, Electrical, Non-Implantable, For Incontinence, a Class II (moderate risk) device regulated under 21 CFR 876.5320.