Last synced on 25 January 2026 at 3:41 am

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

Page Type
Cleared 510(K)
PDF
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
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