Barrx Medical, Incorporated is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Barrx Medical, Incorporated - FDA 510(k) Cleared Devices
13
Total
13
Cleared
0
Denied
Barrx Medical, Incorporated has 13 FDA 510(k) cleared general & plastic surgery devices. Based in Washington, Dc, US.
Historical record: 13 cleared submissions from 2005 to 2010.
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) Regulatory Record - Barrx Medical, Incorporated
13 devices
Cleared
Jan 15, 2010
HALO 360 & SIZING BALLOON, MODEL 3441C
General & Plastic Surgery
30d
Cleared
Jan 08, 2010
HALO ABLATION CATHETER, MODEL 90-9100
General & Plastic Surgery
102d
Cleared
Nov 10, 2009
HALOFLEX ENERGY GENERATOR, MODELS 1190A-115A AND 1190A-230A
General & Plastic Surgery
89d
Cleared
Feb 10, 2009
HALO ABLATION CATHETER
General & Plastic Surgery
56d
Cleared
Feb 02, 2009
MODIFICATION TO: HALO COAGULATION CATHETER, MODELS 32041-18, 32041-20,...
General & Plastic Surgery
49d
Cleared
Oct 08, 2008
HALO360 ENERGY GENERATOR, MODELS 1100C-115B AND 1100C-230B
General & Plastic Surgery
64d
Cleared
Apr 02, 2008
BARRX MODELS HALO360 AND HALO360+ COAGULATION CATHETERS
General & Plastic Surgery
34d
Cleared
Jun 29, 2007
HALO360' COAGULATION CATHETER
General & Plastic Surgery
24d
Cleared
Nov 14, 2006
BARRX HALO COAGULATION SYSTEM
General & Plastic Surgery
85d
Cleared
Nov 09, 2006
HALO90 COAGULATION CATHETER
General & Plastic Surgery
58d
Cleared
Aug 28, 2006
HALO COAGULATION CATHETER
General & Plastic Surgery
26d
Cleared
Apr 21, 2006
BARRX HALO COAGULATION SYSTEM, BARRX HALO COAGULATION GENERATOR, BARRX...
General & Plastic Surgery
88d
Cleared
Jun 29, 2005
BARRX HALO 360 SYSTEM, MODEL 1100C-115A
General & Plastic Surgery
55d