Covidien, Formerly Nellcor Puritan Bennett, Inc. is one of 16087 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Covidien, Formerly Nellcor Puritan Bennett, Inc. - FDA 510(k) Cleared...
Recent clearances: NELLCOR OXIMAX N-600X PULSE OXIMETER, NELLCOR BEDSIDE RESPIRATORY PATIENT MONITORING SYSTEM, NELLCOR BEDSIDE SPO2 PATIEN, VITAL SYNC SYSTEM, 840 VENTILATOR SYSTEM WITH EXPANDED NEOMODE OPTION
5
Total
5
Cleared
0
Denied
Covidien, Formerly Nellcor Puritan Bennett, Inc. has 5 FDA 510(k) cleared medical devices. Based in Boulder, US.
Historical record: 5 cleared submissions from 2008 to 2013. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Covidien, Formerly Nellcor Puritan Bennett, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Covidien, Formerly Nellcor Puritan Bennett, Inc.
5 devices
Cleared
May 09, 2013
NELLCOR OXIMAX N-600X PULSE OXIMETER, NELLCOR BEDSIDE RESPIRATORY PATIENT...
Anesthesiology
170d
Cleared
Feb 27, 2013
VITAL SYNC SYSTEM
Cardiovascular
153d
Cleared
Mar 11, 2010
840 VENTILATOR SYSTEM WITH EXPANDED NEOMODE OPTION
Anesthesiology
176d
Cleared
Apr 02, 2009
PB 840 VENTILATOR SYSTEM WITH LEAK COMPENSATION OPTION, MODEL 840
Anesthesiology
111d
Cleared
Oct 31, 2008
PB 540 VENTILATOR
Anesthesiology
25d