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iVitri EZ

Page Type
Cleared 510(K)
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)
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