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Stentor, Inc.
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
3
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K042292
ISITE PACS
September 8, 2004
K013630
ISITE RADIOLOGY
December 5, 2001
K992698
STENTOR, PAGEVIEW
October 25, 1999