The following data is part of a premarket notification filed by Chattanooga Group, Inc. with the FDA for Forte, Model Cps Ultrasound.
| Device ID | K982829 |
| 510k Number | K982829 |
| Device Name: | FORTE, MODEL CPS ULTRASOUND |
| Classification | Ultrasonic Diathermy For Use In Applying Therapeutic Deep Heat |
| Applicant | CHATTANOOGA GROUP, INC. 4717 ADAMS RD. Hixson, TN 37343 |
| Contact | Joe Elrod |
| Correspondent | Joe Elrod CHATTANOOGA GROUP, INC. 4717 ADAMS RD. Hixson, TN 37343 |
| Product Code | IMI |
| CFR Regulation Number | 890.5300 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1998-08-11 |
| Decision Date | 1998-11-06 |