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 |