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TAUTONA INJECTOR DEVICE

Page Type
Cleared 510(K)
510(k) Number
K131963
510(k) Type
Traditional
Applicant
TAUTONA GROUP, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/22/2013
Days to Decision
117 days
Submission Type
Summary

TAUTONA INJECTOR DEVICE

Page Type
Cleared 510(K)
510(k) Number
K131963
510(k) Type
Traditional
Applicant
TAUTONA GROUP, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/22/2013
Days to Decision
117 days
Submission Type
Summary