FDA 510(k) Applications Submitted by MARY FUNK
FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
K110083 |
01/11/2011 |
V200 VENTILATOR WITH APRV MODE, ESPRIT VENTILATOR WITH APRV MODE |
RESPIRONICS CALIFORNIA, INC. |
K160958 |
04/05/2016 |
Battalion Universal Spacer System |
ALPHATEC SPINE |
K051262 |
05/16/2005 |
ESPRIT VENTILATOR NEONATAL OPTION, MODEL V1000 |
RESPIRONICS CALIFORNIA, INC. |
K041412 |
05/27/2004 |
ESPRIT VENTILATOR WITH NICO-ESPRIT INTERFACE OPTION, MODEL V1000 |
RESPIRONICS CALIFORNIA, INC. |
K022750 |
08/19/2002 |
PLV CONTINUUM VENTILATOR, MODEL P1000 |
RESPIRONICS CALIFORNIA, INC. |
K023350 |
10/07/2002 |
ESPRIT VENTILATOR WITH RESPIRATORY MECHANICS |
RESPIRONICS CALIFORNIA, INC. |
K034032 |
12/29/2003 |
PLV CONTINUUM VENTILATOR, MODEL P2000 |
RESPIRONICS CALIFORNIA, INC. |
K001646 |
05/30/2000 |
PURITAN-BENNETT 840 VENTILATOR SYSTEM WITH NEOMODE OPTION |
PURITAN BENNETT CORP. |
|
|