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SINGLE PHASE DIAGNOSTIC X-RAY GENERATOR FX 350

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K880532
510(k) Type
Traditional
Applicant
FISCHER IMAGING CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/28/1988
Days to Decision
48 days

SINGLE PHASE DIAGNOSTIC X-RAY GENERATOR FX 350

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K880532
510(k) Type
Traditional
Applicant
FISCHER IMAGING CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/28/1988
Days to Decision
48 days