The following data is part of a premarket notification filed by Chattanooga Group, Inc. with the FDA for Intelect 600mp.
| Device ID | K920260 |
| 510k Number | K920260 |
| Device Name: | INTELECT 600MP |
| Classification | Stimulator, Nerve, Transcutaneous, For Pain Relief |
| 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 | GZJ |
| CFR Regulation Number | 882.5890 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1992-01-21 |
| Decision Date | 1992-10-13 |