INTELECT

Stimulator, Muscle, Powered

CHATTANOOGA GROUP, INC.

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

Pre-market Notification Details

• Device ID: K801790
• 510k Number: K801790
• Device Name: INTELECT
• Classification: Stimulator, Muscle, Powered
• Applicant: CHATTANOOGA GROUP, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050
• Product Code: IPF
• CFR Regulation Number: 890.5850 [🔎]
• Decision: Substantially Equivalent (SESE)
• Type: Traditional
• 3rd Party Reviewed: No
• Combination Product: No
• Date Received: 1980-07-29
• Decision Date: 1980-08-20