The following data is part of a premarket notification filed by Chattanooga Group, Inc. with the FDA for Medium Frequ. Elec. Muscle Stimulator.
| Device ID | K850698 |
| 510k Number | K850698 |
| Device Name: | MEDIUM FREQU. ELEC. MUSCLE STIMULATOR |
| Classification | Stimulator, Muscle, Powered |
| Applicant | CHATTANOOGA GROUP, INC. 101 MEMORIAL DR. Red Bank, TN 37405 |
| Contact | Maley |
| Correspondent | Maley CHATTANOOGA GROUP, INC. 101 MEMORIAL DR. Red Bank, TN 37405 |
| Product Code | IPF |
| CFR Regulation Number | 890.5850 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1985-02-21 |
| Decision Date | 1985-05-17 |