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3D IMAGING

Page Type
Cleared 510(K)
510(k) Number
K923823
510(k) Type
Traditional
Applicant
RESONEX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/30/1992
Days to Decision
92 days
Submission Type
Statement

3D IMAGING

Page Type
Cleared 510(K)
510(k) Number
K923823
510(k) Type
Traditional
Applicant
RESONEX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/30/1992
Days to Decision
92 days
Submission Type
Statement