The following data is part of a premarket notification filed by Lsi Intl., Inc. with the FDA for Ms 2500.
| Device ID | K933653 |
| 510k Number | K933653 |
| Device Name: | MS 2500 |
| Classification | Stimulator, Muscle, Powered |
| Applicant | LSI INTL., INC. 8849 BOND Overland Park, KS 66214 |
| Contact | Steve Papa |
| Correspondent | Steve Papa LSI INTL., INC. 8849 BOND Overland Park, KS 66214 |
| Product Code | IPF |
| CFR Regulation Number | 890.5850 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1993-07-28 |
| Decision Date | 1994-03-23 |