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

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

2 devices
1-2 of 2
Cleared Dec 06, 2012
WESTMED, INC.'S BLOCKAIDE FILTER [21 CFR 807.87(A)]
K121382 · CAH
General Hospital · 212d
Cleared Jul 15, 2008
ACCUFLOW AND ACCUFLUX ELASTOMERIC INFUSION PUMP
K081905 · MEB
General Hospital · 12d
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