Medical Device Manufacturer · US , Tucson , AZ

Westmed Intl. - FDA 510(k) Cleared Devices

9 submissions · 9 cleared · Since 1993

Total

Cleared

Denied

Westmed Intl. has 9 FDA 510(k) cleared medical devices. Based in Tucson, US.

Historical record: 9 cleared submissions from 1993 to 1996. Primary specialty: Anesthesiology.

Browse the FDA 510(k) cleared devices submitted by Westmed Intl. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Westmed Intl.

9 devices

1-9 of 9

Cleared Mar 27, 1996

WESTMED CIRCULARIE PEP DEVICES

K955047 · BYE

Anesthesiology · 145d

Cleared Dec 28, 1995

WESTMED CONDESATE COLLECTION TRAP

K954271 · CAW

Anesthesiology · 107d

Cleared Sep 27, 1995

MICROTIME

K952616 · BTI

Anesthesiology · 113d

Cleared Sep 18, 1995

WESTMED PEDIATRIC BACTERIAL/VIRAL FILTER

K953687 · CAH

General Hospital · 42d

Cleared Sep 15, 1995

WESTMED RESPIRATORY LUER ADAPTOR

K953506 · BXY

Anesthesiology · 51d

Cleared Apr 24, 1995

WESTMED BACTERIAL/VIRAL FILTER

K951484 · CAH

General Hospital · 25d

Cleared Feb 07, 1995

WESTMED PEDIATRIC AND ADULT AEROSOL MASK

K945472 · BYG

Anesthesiology · 91d

Cleared Jul 02, 1993

INSTANT IN-DWELL NASAL SUCT TAMP/ALLEVIA NASAL TRA

K924944 · EMX

Ear, Nose, Throat · 275d

Cleared Jan 15, 1993

BOOMERANG TURBINATE GLOVE AND SEPTAL SPLINT

K925173 · LYA

Ear, Nose, Throat · 93d

Westmed Intl. - FDA 510(k) Cleared Devices

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