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Biopor, AOC Porous Polyethylene, Cerepor

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K160988
510(k) Type
Traditional
Applicant
CEREMED, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/14/2016
Days to Decision
97 days
Submission Type
Summary

Biopor, AOC Porous Polyethylene, Cerepor

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K160988
510(k) Type
Traditional
Applicant
CEREMED, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/14/2016
Days to Decision
97 days
Submission Type
Summary