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Fossa Medical, 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
K072293
FOSSA URETERAL OPEN STENTS
August 6, 2008
K033368
FOSSA URETERAL OPEN LUMEN STENT
November 26, 2003
K031292
MODIFICATION TO FOSSA URETERAL STONE SWEEPER
May 22, 2003