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RFX FLUROSCOPIC DIGITAL IMAGING SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K030544
510(k) Type
Traditional
Applicant
SIGMA VISION, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/21/2003
Days to Decision
90 days
Submission Type
Summary

RFX FLUROSCOPIC DIGITAL IMAGING SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K030544
510(k) Type
Traditional
Applicant
SIGMA VISION, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/21/2003
Days to Decision
90 days
Submission Type
Summary