Vectec is one of 5184 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Vectec - FDA 510(k) Cleared Devices
3
Total
3
Cleared
0
Denied
Vectec has 3 FDA 510(k) cleared medical devices. Based in Washington, US.
Historical record: 3 cleared submissions from 2007 to 2013. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Vectec Filter by specialty or product code using the sidebar.
Vectec — FDA 510(k) Products and Clearance History
3 devices
Cleared
Aug 02, 2013
VECTEC DISPOSABLE PNEUMOPERITONEUM NEEDLE
Gastroenterology & Urology
452d
Cleared
Feb 04, 2011
VECTEC DISPOSABLE MONOPOLAR CONNECTOR CABLE
General & Plastic Surgery
46d
Cleared
Sep 06, 2007
VECTEC DISPOSABLE TROCARS AND LAPAROSCOPIC ACCESSORIES
General & Plastic Surgery
51d