3 PHASE HIGH FREQ. DIAG. X-RAY GEN. MICRO-X 60HF— 510(k) K880525

Name: FDA 510(k) clearance K880525
Creator: U.S. Food and Drug Administration
Published: 1988-08-15

Substantially Equivalent

Fischer Imaging Corp.

FDA 510(k) clearance K880525 for 3 PHASE HIGH FREQ. DIAG. X-RAY GEN. MICRO-X 60HF, Substantially Equivalent on 1988-08-15. Applicant: Fischer Imaging Corp.. Device class: 1.

Clearance details

Applicant: Fischer Imaging Corp.
Product code: Code IZO
Device class: Class 1
Regulation: 21 CFR 892.1700
Advisory panel: Radiology
Date received: 1988-02-09
Decision date: 1988-08-15
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Denver, CO, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code IZO

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