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Tesera-K SC System

Page Type
Cleared 510(K)
510(k) Number
K223105
510(k) Type
Traditional
Applicant
Kyocera Medical Technologies, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/22/2022
Days to Decision
83 days
Submission Type
Summary

Tesera-K SC System

Page Type
Cleared 510(K)
510(k) Number
K223105
510(k) Type
Traditional
Applicant
Kyocera Medical Technologies, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/22/2022
Days to Decision
83 days
Submission Type
Summary