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Eastmed, Inc.
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
2
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K083769
MODIFICATION TO URESTA PESSARY
January 14, 2009
K081385
URESTA PESSARY
October 9, 2008