Mallinckrodt Developpement France is one of 283 FDA 510(k) medical device manufacturers from France in the dataset, ranked by real submission volume.
Mallinckrodt Developpement France - FDA 510(k) Cleared Devices
Recent clearances: PURITAN BENNETT, SANDMAN DUO AND SANDMAN DUO ST, SANDMAN INFO WITHOUT HUMIDIFIER/ SANDMAN AUTO WITHOUT HUMIDIFIER, MODEL M-114801-114802-US, SANDMAN INTRO
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.
510(k) submissions have been managed by Kema Quality B.V. as regulatory consultant.
FDA 510(k) Regulatory Record - Mallinckrodt Developpement France
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