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Cryotec

Page Type
Cleared 510(K)
510(k) Number
K162051
510(k) Type
Traditional
Applicant
REPROLIFE INC.
Country
Japan
FDA Decision
Substantially Equivalent
Decision Date
12/14/2016
Days to Decision
142 days
Submission Type
Summary

Cryotec

Page Type
Cleared 510(K)
510(k) Number
K162051
510(k) Type
Traditional
Applicant
REPROLIFE INC.
Country
Japan
FDA Decision
Substantially Equivalent
Decision Date
12/14/2016
Days to Decision
142 days
Submission Type
Summary