INTELECT 210 PORTABLE ULTRASOUND

Ultrasonic Diathermy 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 210 Portable Ultrasound.

Pre-market Notification Details

Device IDK841447
510k NumberK841447
Device Name:INTELECT 210 PORTABLE ULTRASOUND
ClassificationUltrasonic Diathermy For Use In Applying Therapeutic Deep Heat
Applicant CHATTANOOGA GROUP, INC. 803 N. Front St. Suite 3 Mchenry,  IL  60050
Product CodeIMI  
CFR Regulation Number890.5300 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1984-04-06
Decision Date1984-05-09

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