INTELECT 170

Stimulator, Ultrasound And Muscle, For Use In Applying Therapeutic Deep Heat

CHATTANOOGA GROUP, INC.

The following data is part of a premarket notification filed by Chattanooga Group, Inc. with the FDA for Intelect 170.

Pre-market Notification Details

Device IDK902860
510k NumberK902860
Device Name:INTELECT 170
ClassificationStimulator, Ultrasound And Muscle, For Use In Applying Therapeutic Deep Heat
Applicant CHATTANOOGA GROUP, INC. 4717 ADAMS RD. P.O. BOX 4287 Hixson,  TN  37343
ContactGrahame R Watts
CorrespondentGrahame R Watts
CHATTANOOGA GROUP, INC. 4717 ADAMS RD. P.O. BOX 4287 Hixson,  TN  37343
Product CodeIMG  
CFR Regulation Number890.5860 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1990-06-29
Decision Date1990-09-27

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