Medical Device Manufacturer · US , Tucson , AZ

Westmed, Inc. - FDA 510(k) Cleared Devices

8 submissions · 8 cleared · Since 1995

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.

FDA 510(k) Regulatory Record - Westmed, Inc.

8 devices

1-8 of 8

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

Anesthesiology · 13d

Cleared Feb 15, 2007

Anesthesiology · 30d

Cleared Sep 18, 1995

WESTMED PEDIATRIC & ADULT MEDIUM CONCENTRATION OXYGEN MASK

Anesthesiology · 56d