Alaris Medical Systems, Inc. is one of 5795 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Alaris Medical Systems, Inc. - FDA 510(k) Cleared Devices
Recent clearances: MEDLEY PCA MODULE, MODEL 8120, MEDLEY SYSTEM WITH BAR CODE MODULE, MODEL 8600, MEDLEY ETCO2 MODULE (INCLUDES ACCESSORIES), MODEL 8300
16
Total
16
Cleared
0
Denied
Alaris Medical Systems, Inc. has 16 FDA 510(k) cleared medical devices. Based in San Diego, US.
Historical record: 16 cleared submissions from 1998 to 2004. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Alaris Medical Systems, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Alaris Medical Systems, Inc.
16 devices
Cleared
Dec 10, 2004
MEDLEY PCA MODULE, MODEL 8120
General Hospital
10d
Cleared
Jul 06, 2004
MEDLEY SYSTEM WITH BAR CODE MODULE, MODEL 8600
General Hospital
56d
Cleared
Feb 09, 2004
MEDLEY ETCO2 MODULE (INCLUDES ACCESSORIES), MODEL 8300
Anesthesiology
250d
Cleared
Sep 09, 2003
MEDLEY PCA MODULE, MODEL 8120
General Hospital
50d
Cleared
Jul 25, 2003
SIGNATURE EDITION INFUSION PUMP, SIGNATURE EDITION ADMINISTRATION SETS,...
General Hospital
11d
Cleared
Apr 04, 2003
MEDLEY SYSTEM WITH MEDICATION MANAGEMENT SYSTEM (MMS)
General Hospital
52d
Cleared
Dec 19, 2002
MEDLEY SYRINGE PUMP MODULE SYSTEM, MODEL 8110
General Hospital
80d
Cleared
Sep 11, 2002
MEDLEY SPO2 MODULE, MODEL 8210 & SPO2 SENSORS & CABLE
Anesthesiology
30d
Cleared
Aug 06, 2002
ALARIS MEDICAL INFUSION SYSTEM ADMINISTRATION SETS
General Hospital
29d
Cleared
Nov 13, 2001
SINGLE DOSE DISPENSING PIN, MODEL 2201
General Hospital
57d
Cleared
Oct 02, 2001
GEMINI PC-1,PC-2, PC-2TX,PC-4, SIGNATURE EDITION INFUSION PUMP (SE),...
General Hospital
67d
Cleared
Jun 27, 2001
A-LINE AEP MONITOR
Neurology
86d