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Protek Duo Venous Dilator Set, Protek Solo Venous Dilator Set

Page Type
Cleared 510(K)
510(k) Number
K162181
510(k) Type
Traditional
Applicant
CARDIACASSIST INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/6/2017
Days to Decision
155 days
Submission Type
Summary

Protek Duo Venous Dilator Set, Protek Solo Venous Dilator Set

Page Type
Cleared 510(K)
510(k) Number
K162181
510(k) Type
Traditional
Applicant
CARDIACASSIST INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/6/2017
Days to Decision
155 days
Submission Type
Summary