M.K. Meditech Co. , Ltd. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
M.K. Meditech Co. , Ltd. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
M.K. Meditech Co. , Ltd. has 5 FDA 510(k) cleared medical devices. Based in North Attleboro, US.
Historical record: 5 cleared submissions from 2002 to 2005. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by M.K. Meditech Co. , Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - M.K. Meditech Co. , Ltd.
5 devices
Cleared
Apr 05, 2005
INSOSAFE BAK'SNAP RETRACTABLE INSULIN SAFETY SYRINGE
General Hospital
74d
Cleared
Jan 21, 2004
10 ML BAK'SNAP DUOPROSS RETRACTABLE SAFETY SYRINGE
General Hospital
23d
Cleared
Jun 06, 2003
BAK'SNAP DUOPRO SAFETY SYRING (DUOPROSS) SAFETY'TRAY ALLERGY SAFETY SYRINGE TRAY
General Hospital
16d
Cleared
Sep 19, 2002
DUOPRO SAFETY SYRINGE (DUOPROSS)
General Hospital
27d
Cleared
May 02, 2002
DUOPRO SAFETY SYRINGE (DUOPROSS)
General Hospital
65d