TOURNIQUET

Tourniquet, Nonpneumatic

BARRETTA PRODUCTS, RESEARCH AND DEVELOPMENT, INC.

The following data is part of a premarket notification filed by Barretta Products, Research And Development, Inc. with the FDA for Tourniquet.

Pre-market Notification Details

• Device ID: K881398
• 510k Number: K881398
• Device Name: TOURNIQUET
• Classification: Tourniquet, Nonpneumatic
• Applicant: BARRETTA PRODUCTS, RESEARCH AND DEVELOPMENT, INC. 130 DURHU DRIVE, DEPT. D Mobile, AL 36608
• Contact: Carl Barrett
• Correspondent: Carl Barrett; BARRETTA PRODUCTS, RESEARCH AND DEVELOPMENT, INC. 130 DURHU DRIVE, DEPT. D Mobile, AL 36608
• Product Code: GAX
• CFR Regulation Number: 878.5900 [🔎]
• Decision: Substantially Equivalent (SESE)
• Type: Traditional
• 3rd Party Reviewed: No
• Combination Product: No
• Date Received: 1988-04-04
• Decision Date: 1988-04-29