WRENCH

Wrench

TRUTH, INC.

The following data is part of a premarket notification filed by Truth, Inc. with the FDA for Wrench.

Pre-market Notification Details

• Device ID: K791073
• 510k Number: K791073
• Device Name: WRENCH
• Classification: Wrench
• Applicant: TRUTH, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050
• Product Code: HXC
• CFR Regulation Number: 888.4540 [🔎]
• Decision: Substantially Equivalent (SESE)
• Type: Traditional
• 3rd Party Reviewed: No
• Combination Product: No
• Date Received: 1979-06-12
• Decision Date: 1979-06-20