Mallinckrodt Developpement France - FDA 510(k) Cleared Devices
7
Total
7
Cleared
0
Denied
Mallinckrodt Developpement France has 7 FDA 510(k) cleared medical devices. Based in Villers-Les-Nancy Cedex, FR.
Historical record: 7 cleared submissions from 2000 to 2008. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Mallinckrodt Developpement France Filter by specialty or product code using the sidebar.
7 devices
Cleared
Oct 09, 2008
PURITAN BENNETT, SANDMAN DUO AND SANDMAN DUO ST
Anesthesiology
63d
Cleared
May 16, 2008
SANDMAN INFO WITHOUT HUMIDIFIER/ SANDMAN AUTO WITHOUT HUMIDIFIER, MODEL...
Anesthesiology
87d
Cleared
Sep 10, 2007
SANDMAN INTRO
Anesthesiology
94d
Cleared
Apr 06, 2007
KNIGHTCONTROL REMOTE CONTROL, MODEL M-114700-US
Anesthesiology
137d
Cleared
Jan 10, 2005
GOODKNIGHT H20, MODEL M-114600-00
Anesthesiology
151d
Cleared
Jul 22, 2004
GOODKNIGHT 425, MODELM-114500-00
Anesthesiology
16d
Cleared
Jul 05, 2000
MALLINCKRODT, GOODKNIGHT 418S
Anesthesiology
16d