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OSIRIX MD

Page Type
Cleared 510(K)
510(k) Number
K101342
510(k) Type
Traditional
Applicant
PIXMEO SARL
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/20/2010
Days to Decision
99 days
Submission Type
Summary

OSIRIX MD

Page Type
Cleared 510(K)
510(k) Number
K101342
510(k) Type
Traditional
Applicant
PIXMEO SARL
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/20/2010
Days to Decision
99 days
Submission Type
Summary