Last synced on 25 January 2026 at 3:41 am

3D IMAGING

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
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