The following data is part of a premarket notification filed by Chattanooga Group, Inc. with the FDA for Intelect Ifc2.
Device ID | K924666 |
510k Number | K924666 |
Device Name: | INTELECT IFC2 |
Classification | Interferential Current Therapy |
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 | LIH |
CFR Regulation Number | 882.5890 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1992-09-16 |
Decision Date | 1993-03-05 |