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GEMINI STANDARD AND MINI VALVES

Page Type
Cleared 510(K)
510(k) Number
K974708
510(k) Type
Traditional
Applicant
NEUROCARE GROUP
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/10/1998
Days to Decision
83 days
Submission Type
Summary

GEMINI STANDARD AND MINI VALVES

Page Type
Cleared 510(K)
510(k) Number
K974708
510(k) Type
Traditional
Applicant
NEUROCARE GROUP
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/10/1998
Days to Decision
83 days
Submission Type
Summary