Premarket Approval (PMA)

Note: This medical device record is a PMA supplement. A supplement may have changed the device description/function or indication from that approved in the original PMA. Be sure to look at the original PMA record for more information.

• Device: Angio Seal Vascular Closure Device
• Generic Name: Device, hemostasis, vascular
• Applicant: Terumo Medical Corporation; 950 Elkton Blvd.; Elkton, MD 21921
• PMA Number: P930038
• Supplement Number: S089
• Date Received: 07/16/2018
• Decision Date: 08/15/2018
• Product Code: MGB
• Advisory Committee: Cardiovascular
• Supplement Type: 30-Day Notice
• Supplement Reason: Process Change - Manufacturer/Sterilizer/Packager/Supplier
• Expedited Review Granted?: No
• Combination Product: No
• Predetermined Change Control Plan Authorized: No

Approval Order Statement  
Transfer the carrier tube component manufacturing process to the Puerto Rico facility.