PMA P990037S018

Device: DUETT PRO SEALING DEVICE, DIAGNOSTIC DUETT PRO SEALING DEVICE AND D-STAT FLOWABLE HEMOSTAT
Applicant: Vascular Solutions, Inc.
PMA number: P990037
Supplement: S018
Product code: MGB
Decision date: 2003-05-27
Classification: Device, Hemostasis, Vascular
Generic name: Device, hemostasis, vascular
Approval order statement: APPROVAL FOR A MANUFACTURING SITE LOCATED AT VASCULAR SOLUTIONS, INC., MINNEAPOLIS, MINNESOTA.

Current openFDA PMA Record#

Device: DUETT PRO SEALING DEVICE, DIAGNOSTIC DUETT PRO SEALING DEVICE AND D-STAT FLOWABLE HEMOSTAT
Applicant: Vascular Solutions, Inc.
PMA number: P990037
Supplement: S018
Product code: MGB
Generic name: Device, hemostasis, vascular
Decision date: 2003-05-27
Decision code: APPR
Date received: 2003-04-30
Supplement type: Normal 180 Day Track No User Fee
Supplement reason: Location Change - Manufacturer/Sterilizer/Packager/Supplier
Approval order statement: APPROVAL FOR A MANUFACTURING SITE LOCATED AT VASCULAR SOLUTIONS, INC., MINNEAPOLIS, MINNESOTA.