CSA Medical, Inc. - FDA 510(k) Cleared Devices
14
Total
14
Cleared
0
Denied
CSA Medical, Inc. has 14 FDA 510(k) cleared general & plastic surgery devices. Based in Baltimore, US.
Historical record: 14 cleared submissions from 2007 to 2020.
Browse the complete list of FDA 510(k) cleared general & plastic surgery devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by CSA Medical, Inc.
14 devices
Cleared
Dec 07, 2020
Vortex Radial Spray Catheter
General & Plastic Surgery
220d
Cleared
Aug 30, 2017
truFreeze System
General & Plastic Surgery
89d
Cleared
Jul 27, 2017
truFreeze System
General & Plastic Surgery
21d
Cleared
Jul 14, 2017
truFreeze Rapid AV Spray Kit
General & Plastic Surgery
50d
Cleared
May 24, 2017
truFreeze System
General & Plastic Surgery
187d
Cleared
Oct 25, 2016
truFreeze System
General & Plastic Surgery
28d
Cleared
Jul 26, 2016
truFreeze System
General & Plastic Surgery
50d
Cleared
Oct 14, 2015
truFreeze System
General & Plastic Surgery
27d
Cleared
Jun 17, 2015
truFreeze System
General & Plastic Surgery
72d
Cleared
Jan 15, 2015
truFreeze System
General & Plastic Surgery
24d
Cleared
Jun 19, 2014
TRUFREEZE SYSTEM
General & Plastic Surgery
239d
Cleared
Feb 07, 2012
TRUFREEZE SYSTEM, TRUFREEZE SPRAY KIT
General & Plastic Surgery
119d
Cleared
Dec 07, 2007
CRYOSPRAY ABLATION SYSTEM, MODEL CC2-NAM
General & Plastic Surgery
79d
Cleared
May 01, 2007
CRYOSPRAY ABLATION SYSTEM, MODEL CU 8407020500
General & Plastic Surgery
32d