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DYNA VUE 3-D IMAGING PRODUCT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K974755
510(k) Type
Traditional
Applicant
IMD SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/4/1998
Days to Decision
75 days
Submission Type
Summary

DYNA VUE 3-D IMAGING PRODUCT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K974755
510(k) Type
Traditional
Applicant
IMD SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/4/1998
Days to Decision
75 days
Submission Type
Summary