Msb , Ltd. is one of 195 FDA 510(k) medical device manufacturers from United Kingdom in the dataset, ranked by real submission volume.
Msb , Ltd. - FDA 510(k) Cleared Devices
7
Total
7
Cleared
0
Denied
Msb , Ltd. has 7 FDA 510(k) cleared medical devices. Based in Marlborough, Wiltshire, GB.
Historical record: 7 cleared submissions from 1994 to 1998. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Msb , Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Msb , Ltd.
7 devices
Cleared
Feb 27, 1998
MSB TENS ELECTRODES (DISPOSABLE)
Neurology
36d
Cleared
May 17, 1996
UNILECT, MONITAB AND BIOTRACE-HR
Cardiovascular
612d
Cleared
May 16, 1996
BIOTRACE-N, NS, 410 AND RT
Cardiovascular
611d
Cleared
Jan 30, 1996
NEUTRALECT ADULT STANDARD, RETURN (REM) & PAEDIATRIC ELECTROSURGERY PLATE...
General & Plastic Surgery
82d
Cleared
Oct 16, 1995
ECOTABS
Cardiovascular
249d
Cleared
Jul 07, 1995
ECG ELECTRODE
Cardiovascular
311d
Cleared
Nov 09, 1994
NEUTRALECT ADULT STANDARD, RETURN (REM), PAEDIATRIC STANDARD, RETURN (REM)
General & Plastic Surgery
41d