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Alveolus, Inc.

FDA Regulatory Profile

Alveolus, Inc. appears in FDA public data with 0 recalls, 12 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on March 11, 2009.

Summary

Total Recalls
0
510(k) Clearances
12
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K083625AERO DV TRACHEOBRONCHIAL STENT SYSTEMMarch 11, 2009
K082284AERO TRACHEOBRONCHIAL STENT TECHNOLOGY SYSTEMNovember 20, 2008
K080838ALVEOLUS ALIMAXX-E ESOPHAGEAL STENT SYSTEMApril 24, 2008
K072720ALIMAXX-B UNCOVERED BILIARY STENT SYSTEMApril 11, 2008
K071604ALVEOLUS AERO DV TRACHEOBRONCHIAL STENT SYSTEMSeptember 19, 2007
K062511AERO TRACHEOBRONCHIAL STENT SYSTEM, MODEL 90129-2XXJanuary 31, 2007
K060239ALEOLUS/ENOVENTIONS,ALIMAXX-E DV ESOPHAGEAL STENT SYSTEMMarch 22, 2006
K051621ENDOVENTIONS ALIMAXX-E ESOPHAGEAL STENT SYSTEMJuly 11, 2005
K033990ALVEOLUS INC. TB-STS TRACHEOBRONCHIAL STENT SYSTEMMay 12, 2004
K033053ALVEOLUS, TB-STS TRACHEOBRONCHIAL STENT SYSTEMFebruary 25, 2004
K032744ALVEOLUS INC., TB-STS TRACHEOBRONCHIAL STENT SYSTEMNovember 13, 2003
K030947ALVEOLUS INC., TB-STS TRACHEOBRONCHIAL STENT SYSTEMMay 15, 2003

FDA data resources