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

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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