Medimop Medical Projects, Ltd. is one of 4790 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Medimop Medical Projects, Ltd. - FDA 510(k) Cleared Devices
12
Total
12
Cleared
0
Denied
Medimop Medical Projects, Ltd. has 12 FDA 510(k) cleared general hospital devices. Based in Washington, US.
Historical record: 12 cleared submissions from 1996 to 2016.
Browse the complete list of FDA 510(k) cleared general hospital devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Medimop Medical Projects, Ltd.
12 devices
Cleared
May 04, 2016
Vented Vial Adapter Transfer Device - 13mm
General Hospital
70d
Cleared
Jun 12, 2014
VIAL2BAG DIRECT CONNECT
General Hospital
80d
Cleared
Aug 08, 2013
MP VIAL ADAPTER 13MM
General Hospital
195d
Cleared
Jul 31, 2013
VIAL CONNECTOR 13MM CLOSED COLLAR
General Hospital
29d
Cleared
Oct 04, 2012
MIXJECT WITH SPRAY HEAD
General Hospital
85d
Cleared
Dec 13, 2007
SWABABLE VIAL ADAPTER 13MM, SWABABLE VIAL ADAPTER 20MM
General Hospital
98d
Cleared
Dec 13, 2007
VIAL2BAG
General Hospital
76d
Cleared
Nov 03, 2006
VENTED VIAL ADAPTER TRANSFER DEVICE
General Hospital
71d
Cleared
Jul 29, 2003
MIX2VIAL TRANSFER DEVICE
General Hospital
43d
Cleared
Jul 11, 2000
NEEDLELESS TRANSFER DEVICE
General Hospital
25d
Cleared
May 05, 2000
MODIFICATION TO MIXJECT DISPENSING PIN/WITH DETACHABLE VIAL HOLDER/WITH...
General Hospital
11d
Cleared
Oct 07, 1996
MIXJECT DISPENSING PIN/WITH DETACHABLE VIAL HOLDER/WITH DETACHABLE VIAL...
General Hospital
31d