Halifax Biomedical, Inc. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Halifax Biomedical, Inc. has 5 FDA 510(k) cleared medical devices. Based in Dundas, CA.
Historical record: 5 cleared submissions from 2009 to 2018. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Halifax Biomedical, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Halifax Biomedical, Inc.
5 devices
Cleared
Oct 31, 2018
Halifax Imaging Kit
Radiology
16d
Cleared
Mar 06, 2014
MODEL-BASED RSA SOFTWARE
Radiology
72d
Cleared
Jun 01, 2012
SR SUITE 1.0
Radiology
28d
Cleared
Jun 28, 2011
HALIFAX BIOMEDICAL TANATLUM BEAD SET
General & Plastic Surgery
218d
Cleared
Aug 21, 2009
TANTALUM BEAD SET, MODEL P003175
General & Plastic Surgery
171d