Z-Medica Corporation is one of 5250 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Z-Medica Corporation - FDA 510(k) Cleared Devices
8
Total
8
Cleared
0
Denied
Z-Medica Corporation has 8 FDA 510(k) cleared medical devices. Based in Wallingford, US.
Historical record: 8 cleared submissions from 2005 to 2013. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Z-Medica Corporation Filter by specialty or product code using the sidebar.
Z-Medica Corporation — FDA 510(k) Products and Clearance History
8 devices
Cleared
Mar 20, 2013
INTERVENTIONAL HEMOSTATIC BANDAGE
General & Plastic Surgery
370d
Cleared
Apr 08, 2009
QUIKCLOT INTEVENTIONAL, MODEL P/N 182
General & Plastic Surgery
30d
Cleared
Feb 27, 2008
QUIKCLOT NOSEBLEED
General & Plastic Surgery
27d
Cleared
Oct 16, 2007
QUIKCLOT EX
General & Plastic Surgery
42d
Cleared
Jan 25, 2007
QUIKCLOT SPORT AND QUIKCLOT SPORT SILVER
General & Plastic Surgery
22d
Cleared
Jul 19, 2006
QUIKCLOT 1ST RESPONSE & QUIKCLOT ACS+
General & Plastic Surgery
26d
Cleared
Aug 10, 2005
QUICKCLOT ACS - ACCELERATED CLOTTING SPONGE
General & Plastic Surgery
22d
Cleared
Apr 14, 2005
QUIKCLOT BRAND HEMOSTATIC AGENT - ADVANCED BEADED FORMULATION - 100G - 1.9MM...
General & Plastic Surgery
20d