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Gemini XXP-HP

Page Type
Cleared 510(K)
510(k) Number
K151298
510(k) Type
Traditional
Applicant
Dornier Medtech America
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/30/2015
Days to Decision
76 days
Submission Type
Summary

Gemini XXP-HP

Page Type
Cleared 510(K)
510(k) Number
K151298
510(k) Type
Traditional
Applicant
Dornier Medtech America
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/30/2015
Days to Decision
76 days
Submission Type
Summary