INTELECT

Stimulator, Nerve, Transcutaneous, For Pain Relief

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: K974497
• 510k Number: K974497
• Device Name: INTELECT
• Classification: Stimulator, Nerve, Transcutaneous, For Pain Relief
• Applicant: CHATTANOOGA GROUP, INC. 4717 ADAMS RD. P.O. BOX 4287 Hixson, TN 37343
• Contact: Joe Elrod
• Correspondent: Joe Elrod; CHATTANOOGA GROUP, INC. 4717 ADAMS RD. P.O. BOX 4287 Hixson, TN 37343
• Product Code: GZJ
• Subsequent Product Code: IPF
• Subsequent Product Code: LIH
• CFR Regulation Number: 882.5890 [🔎]
• Decision: Substantially Equivalent (SESE)
• Type: Traditional
• 3rd Party Reviewed: No
• Combination Product: No
• Date Received: 1997-11-28
• Decision Date: 1998-01-23