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THREE PHASE, DIAGNOSTIC X-RAY GENERATOR MICRO-X 80

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K880522
510(k) Type
Traditional
Applicant
FISCHER IMAGING CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/4/1988
Days to Decision
85 days

THREE PHASE, DIAGNOSTIC X-RAY GENERATOR MICRO-X 80

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K880522
510(k) Type
Traditional
Applicant
FISCHER IMAGING CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/4/1988
Days to Decision
85 days