The following data is part of a premarket notification filed by Empi with the FDA for Minnova Pelvic Floor Stimulation System.
| Device ID | K970307 |
| 510k Number | K970307 |
| Device Name: | MINNOVA PELVIC FLOOR STIMULATION SYSTEM |
| Classification | Stimulator, Electrical, Non-implantable, For Incontinence |
| Applicant | EMPI 599 CARDIGAN RD. St. Paul, MN 55126 |
| Contact | Carolyn M Steele Husten |
| Correspondent | Carolyn M Steele Husten EMPI 599 CARDIGAN RD. St. Paul, MN 55126 |
| Product Code | KPI |
| CFR Regulation Number | 876.5320 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1997-01-27 |
| Decision Date | 1997-04-22 |
| Summary: | summary |