Last synced on 18 April 2025 at 11:05 pm

ETIII SA Fixture System (O3.2mm)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K153332
510(k) Type
Traditional
Applicant
HIOSSEN INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/27/2016
Days to Decision
343 days
Submission Type
Summary

ETIII SA Fixture System (O3.2mm)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K153332
510(k) Type
Traditional
Applicant
HIOSSEN INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/27/2016
Days to Decision
343 days
Submission Type
Summary