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Oclet TDS 1000

Page Type
Cleared 510(K)
510(k) Number
K212049
510(k) Type
Traditional
Applicant
TendoNova Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/8/2022
Days to Decision
251 days
Submission Type
Summary

Oclet TDS 1000

Page Type
Cleared 510(K)
510(k) Number
K212049
510(k) Type
Traditional
Applicant
TendoNova Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/8/2022
Days to Decision
251 days
Submission Type
Summary