Board of Directors, Albert Browne , Ltd. is one of 195 FDA 510(k) medical device manufacturers from United Kingdom in the dataset, ranked by real submission volume.
Board of Directors, Albert Browne , Ltd. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Board of Directors, Albert Browne , Ltd. has 5 FDA 510(k) cleared medical devices. Based in Leics. Le4 Oaa, GB.
Historical record: 5 cleared submissions from 1990 to 1998. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Board of Directors, Albert Browne , Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Board of Directors, Albert Browne , Ltd.
5 devices
Cleared
Jul 10, 1998
BROWNE TST SINGLE USE BOWIE-DICK TYPE TEST PACK
General Hospital
407d
Cleared
Jun 24, 1997
BROWNE STEAM INDICATOR
General Hospital
104d
Cleared
Aug 05, 1994
BROWNE TST SINGLE USE BOWIE DICK TYPE TEST PACK
General Hospital
464d
Cleared
Jun 02, 1994
BROWNE GA INDICATOR USE IN 2% ACTIV GLUTARALDEHYDE
General Hospital
737d
Cleared
Nov 01, 1990
TST CONTROL INTEGRATOR FOR STEAM AUTOCLAVE
General Hospital
119d