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Zutron Medical, LLC
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
2
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K093718
ZUTRON MEDICAL ENDOSCOPE LEAK TESTER MODEL ZUTR-10003
February 22, 2010
K051068
ZUTRON COLONOSCOPE STIFFENING DEVICE
July 11, 2005