The following data is part of a premarket notification filed by Chattanooga Group, Inc. with the FDA for Emg Retrainer.
| Device ID | K972487 |
| 510k Number | K972487 |
| Device Name: | EMG RETRAINER |
| Classification | Device, Biofeedback |
| Applicant | CHATTANOOGA GROUP, INC. 4717 ADAMS RD. P.O. BOX 489 Hixson, TN 37343 -0489 |
| Contact | Joe Elrod |
| Correspondent | Joe Elrod CHATTANOOGA GROUP, INC. 4717 ADAMS RD. P.O. BOX 489 Hixson, TN 37343 -0489 |
| Product Code | HCC |
| CFR Regulation Number | 882.5050 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1997-07-02 |
| Decision Date | 1997-09-26 |
| Summary: | summary |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() EMG RETRAINER 75273616 2188549 Dead/Cancelled |
ENCORE MEDICAL ASSET CORPORATION 1997-04-14 |