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IMLOGIX 1000 IMAGE DISPLAY SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K893521
510(k) Type
Traditional
Applicant
IMLOGIX A DIV. OF MICROTERM
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/23/1989
Days to Decision
46 days

IMLOGIX 1000 IMAGE DISPLAY SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K893521
510(k) Type
Traditional
Applicant
IMLOGIX A DIV. OF MICROTERM
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/23/1989
Days to Decision
46 days