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Circumplast Circumcision Device

Page Type
Cleared 510(K)
510(k) Number
K151095
510(k) Type
Traditional
Applicant
Novadien Healthcare
Country
Australia
FDA Decision
Substantially Equivalent
Decision Date
9/18/2015
Days to Decision
148 days
Submission Type
Summary

Circumplast Circumcision Device

Page Type
Cleared 510(K)
510(k) Number
K151095
510(k) Type
Traditional
Applicant
Novadien Healthcare
Country
Australia
FDA Decision
Substantially Equivalent
Decision Date
9/18/2015
Days to Decision
148 days
Submission Type
Summary