FORTE

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 Forte.

Pre-market Notification Details

• Device ID: K953614
• 510k Number: K953614
• Device Name: FORTE
• Classification: Stimulator, Ultrasound And Muscle, For Use In Applying Therapeutic Deep Heat
• 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: IMG
• Subsequent Product Code: GZK
• Subsequent Product Code: IMI
• Subsequent Product Code: IPF
• Subsequent Product Code: LIH
• CFR Regulation Number: 890.5860 [🔎]
• Decision: Substantially Equivalent For Some Indications (SN)
• Type: Traditional
• 3rd Party Reviewed: No
• Combination Product: No
• Date Received: 1995-08-03
• Decision Date: 1995-10-27