Last synced on 26 May 2023 at 11:04 pm

iVitri EZ

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K162640
510(k) Type
Traditional
Applicant
REPROBITECH CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/30/2017
Days to Decision
281 days
Submission Type
Summary

iVitri EZ

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K162640
510(k) Type
Traditional
Applicant
REPROBITECH CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/30/2017
Days to Decision
281 days
Submission Type
Summary