The following data is part of a premarket notification filed by Midwest Development with the FDA for Ft2000 Sequencer For Muscle Stimulator.
| Device ID | K050595 |
| 510k Number | K050595 |
| Device Name: | FT2000 SEQUENCER FOR MUSCLE STIMULATOR |
| Classification | Stimulator, Muscle, Powered |
| Applicant | MIDWEST DEVELOPMENT S65 W35739 PIPER ROAD Eagle, WI 53119 |
| Contact | Stephen Gorski |
| Correspondent | Stephen Gorski MIDWEST DEVELOPMENT S65 W35739 PIPER ROAD Eagle, WI 53119 |
| Product Code | IPF |
| CFR Regulation Number | 890.5850 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2005-03-08 |
| Decision Date | 2005-05-23 |
| Summary: | summary |