The following data is part of a premarket notification filed by Chattanooga Group, Inc. with the FDA for Electro-goniometer Diagnostic Device.
| Device ID | K901290 |
| 510k Number | K901290 |
| Device Name: | ELECTRO-GONIOMETER DIAGNOSTIC DEVICE |
| Classification | Dynamometer, Ac-powered |
| Applicant | CHATTANOOGA GROUP, INC. 4717 ADAMS RD. P.O. BOX 4287 Hixson, TN 37343 |
| Contact | Grahame R Watts |
| Correspondent | Grahame R Watts CHATTANOOGA GROUP, INC. 4717 ADAMS RD. P.O. BOX 4287 Hixson, TN 37343 |
| Product Code | LBB |
| CFR Regulation Number | 888.1240 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1990-03-20 |
| Decision Date | 1990-10-01 |