THREE PHASE, DIAGNOSTIC GENERATOR MICRO-X 75— 510(k) K880523

Substantially Equivalent

Fischer Imaging Corp.

FDA 510(k) clearance K880523 for THREE PHASE, DIAGNOSTIC GENERATOR MICRO-X 75, 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

Download summary PDF View on FDA.gov ↗

Data sourced from openFDA. This site is unofficial and independent of the FDA.