THREE PHASE, DIAGNOSTIC X-RAY GENERATOR MICRO-X 80— 510(k) K880522

Substantially Equivalent

Fischer Imaging Corp.

FDA 510(k) clearance K880522 for THREE PHASE, DIAGNOSTIC X-RAY GENERATOR MICRO-X 80, Substantially Equivalent on 1988-05-04. Applicant: Fischer Imaging Corp..

Clearance details

Applicant: Fischer Imaging Corp.
Product code: Code IZO
Advisory panel: Radiology
Date received: 1988-02-09
Decision date: 1988-05-04
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Denver, CO, US

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