KONICA QX-130APLUS AUTOMATIC X-RAY FILM PROCESSOR— 510(k) K931313

Name: FDA 510(k) clearance K931313
Creator: U.S. Food and Drug Administration
Published: 1993-09-07

Substantially Equivalent

Konica Medical Corp.

FDA 510(k) clearance K931313 for KONICA QX-130APLUS AUTOMATIC X-RAY FILM PROCESSOR, Substantially Equivalent on 1993-09-07. Applicant: Konica Medical Corp.. Device class: 2.

Clearance details

Applicant: Konica Medical Corp.
Product code: Code IXW
Device class: Class 2
Regulation: 21 CFR 892.1900
Advisory panel: Radiology
Date received: 1993-03-15
Decision date: 1993-09-07
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Washington, DC, US

Download summary PDF View on FDA.gov ↗

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