Last synced on 14 November 2025 at 11:06 pm

ZIRMON SERIES

Page Type
Cleared 510(K)
510(k) Number
K131117
510(k) Type
Traditional
Applicant
KUWOTECH CO., LTD
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/26/2013
Days to Decision
95 days
Submission Type
Summary

ZIRMON SERIES

Page Type
Cleared 510(K)
510(k) Number
K131117
510(k) Type
Traditional
Applicant
KUWOTECH CO., LTD
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/26/2013
Days to Decision
95 days
Submission Type
Summary