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Hem-Avert Perianal Stabilizer

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
DEN160005
510(k) Type
Direct
Applicant
STETRIX, INC.
Country
United States
FDA Decision
Deleted
Decision Date
12/19/2016
Days to Decision
326 days

Hem-Avert Perianal Stabilizer

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
DEN160005
510(k) Type
Direct
Applicant
STETRIX, INC.
Country
United States
FDA Decision
Deleted
Decision Date
12/19/2016
Days to Decision
326 days