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Cresilon Hemostatic Gel, CHG, Cresilon Hemostatic Gel (CHG)

Page Type
Cleared 510(K)
510(k) Number
K213652
510(k) Type
Traditional
Applicant
Cresilon, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/28/2023
Days to Decision
586 days
Submission Type
Summary

Cresilon Hemostatic Gel, CHG, Cresilon Hemostatic Gel (CHG)

Page Type
Cleared 510(K)
510(k) Number
K213652
510(k) Type
Traditional
Applicant
Cresilon, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/28/2023
Days to Decision
586 days
Submission Type
Summary