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3 PHASE HIGH FREQ. DIAG. X-RAY GEN. MICRO-X 60HF

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K880525
510(k) Type
Traditional
Applicant
FISCHER IMAGING CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/15/1988
Days to Decision
188 days

3 PHASE HIGH FREQ. DIAG. X-RAY GEN. MICRO-X 60HF

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K880525
510(k) Type
Traditional
Applicant
FISCHER IMAGING CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/15/1988
Days to Decision
188 days