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GENTLE COLON (REVISION 2.0)

Page Type
Cleared 510(K)
510(k) Number
K061532
510(k) Type
Traditional
Applicant
RENDOSCOPY, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/18/2006
Days to Decision
108 days
Submission Type
Summary

GENTLE COLON (REVISION 2.0)

Page Type
Cleared 510(K)
510(k) Number
K061532
510(k) Type
Traditional
Applicant
RENDOSCOPY, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/18/2006
Days to Decision
108 days
Submission Type
Summary