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ZUTRON COLONOSCOPE STIFFENING DEVICE

Page Type
Cleared 510(K)
510(k) Number
K051068
510(k) Type
Traditional
Applicant
ZUTRON MEDICAL
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/11/2005
Days to Decision
76 days
Submission Type
Summary

ZUTRON COLONOSCOPE STIFFENING DEVICE

Page Type
Cleared 510(K)
510(k) Number
K051068
510(k) Type
Traditional
Applicant
ZUTRON MEDICAL
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/11/2005
Days to Decision
76 days
Submission Type
Summary