Westmed, Inc. is one of 18344 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Westmed, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Westmed Gas Sampling Cannula with O2 delivery, Disposable Pressure Manometer (DPM), VIBRALUNG ACOUSTICAL PERCUSSOR
8
Total
8
Cleared
0
Denied
Westmed, Inc. has 8 FDA 510(k) cleared medical devices. Based in Tucson, US.
Historical record: 8 cleared submissions from 1995 to 2016. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Westmed, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Intertek Testing Services as regulatory consultant.
FDA 510(k) Regulatory Record - Westmed, Inc.
8 devices
Cleared
Dec 14, 2016
Westmed Gas Sampling Cannula with O2 delivery
Anesthesiology
114d
Cleared
Aug 11, 2015
Disposable Pressure Manometer (DPM)
Anesthesiology
281d
Cleared
May 23, 2014
VIBRALUNG ACOUSTICAL PERCUSSOR
Anesthesiology
238d
Cleared
Dec 06, 2012
WESTMED, INC.'S BLOCKAIDE FILTER [21 CFR 807.87(A)]
General Hospital
212d
Cleared
Jul 15, 2008
ACCUFLOW AND ACCUFLUX ELASTOMERIC INFUSION PUMP
General Hospital
12d
Cleared
Aug 23, 2007
PEDI CO2 EASY
Anesthesiology
13d
Cleared
Feb 15, 2007
CO2 EASY
Anesthesiology
30d
Cleared
Sep 18, 1995
WESTMED PEDIATRIC & ADULT MEDIUM CONCENTRATION OXYGEN MASK
Anesthesiology
56d