The following data is part of a premarket notification filed by Chattanooga Group with the FDA for Vitalstim Experia.
| Device ID | K070425 |
| 510k Number | K070425 |
| Device Name: | VITALSTIM EXPERIA |
| Classification | Stimulator, Muscle, Powered |
| Applicant | CHATTANOOGA GROUP 4717 ADAMS RD. Hixson, TN 37343 |
| Contact | Michael Treas |
| Correspondent | Michael Treas CHATTANOOGA GROUP 4717 ADAMS RD. Hixson, TN 37343 |
| Product Code | IPF |
| CFR Regulation Number | 890.5850 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2007-02-13 |
| Decision Date | 2007-06-11 |
| Summary: | summary |