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Cuptimize

Page Type
Cleared 510(K)
510(k) Number
K203651
510(k) Type
Traditional
Applicant
Cuptimize, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/26/2021
Days to Decision
74 days
Submission Type
Summary

Cuptimize

Page Type
Cleared 510(K)
510(k) Number
K203651
510(k) Type
Traditional
Applicant
Cuptimize, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/26/2021
Days to Decision
74 days
Submission Type
Summary