Roxwood Medical, Inc. is one of 4730 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Roxwood Medical, Inc. - FDA 510(k) Cleared Devices
8
Total
8
Cleared
0
Denied
Roxwood Medical, Inc. has 8 FDA 510(k) cleared medical devices. Based in San Francisco, US.
Historical record: 8 cleared submissions from 2012 to 2017. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Roxwood Medical, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Roxwood Medical, Inc.
8 devices
Cleared
Mar 07, 2017
CenterCross Ultra LV Catheter
Cardiovascular
26d
Cleared
Jun 17, 2016
CenterCross Ultra Catheter
Cardiovascular
99d
Cleared
Mar 04, 2016
MultiCross Catheter
Cardiovascular
149d
Cleared
Jan 26, 2016
CenterCross Ultra Catheter
Cardiovascular
151d
Cleared
Jun 07, 2015
MicroCross Catheter
Cardiovascular
46d
Cleared
Apr 14, 2015
MicroCross Catheter
Cardiovascular
104d
Cleared
Nov 19, 2014
CENTERCROSS CATHETER
Cardiovascular
224d
Cleared
Nov 27, 2012
MULTICROSS SUPPORT CATHETER
Cardiovascular
165d