Medical Device Manufacturer · FR , Villers-Les-Nancy Cedex

Mallinckrodt Developpement France - FDA 510(k) Cleared Devices

7 submissions · 7 cleared · Since 2000

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

View 7 510(k) Devices ↓
7
Total
7
Cleared
0
Denied

FDA 510(k) Regulatory Record - Mallinckrodt Developpement France Anesthesiology ✕

7 devices
1-7 of 7
Cleared Oct 09, 2008
PURITAN BENNETT, SANDMAN DUO AND SANDMAN DUO ST
K082237 · BZD
Anesthesiology · 63d
Cleared May 16, 2008
SANDMAN INFO WITHOUT HUMIDIFIER/ SANDMAN AUTO WITHOUT HUMIDIFIER, MODEL...
K080439 · BZD
Anesthesiology · 87d
Cleared Sep 10, 2007
SANDMAN INTRO
K071575 · BZD
Anesthesiology · 94d
Cleared Apr 06, 2007
KNIGHTCONTROL REMOTE CONTROL, MODEL M-114700-US
K063501 · BZD
Anesthesiology · 137d
Cleared Jan 10, 2005
GOODKNIGHT H20, MODEL M-114600-00
K042184 · BTT
Anesthesiology · 151d
Cleared Jul 22, 2004
GOODKNIGHT 425, MODELM-114500-00
K041819 · BZD
Anesthesiology · 16d
Cleared Jul 05, 2000
MALLINCKRODT, GOODKNIGHT 418S
K001845 · BZD
Anesthesiology · 16d
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