AGFA DIAGNOSTIC CENTER ADC, ADC COMPACT, AND ADC SOLO— 510(k) K000159

Name: FDA 510(k) clearance K000159
Creator: U.S. Food and Drug Administration
Published: 2000-02-16

Substantially Equivalent

Agfa Corp.

FDA 510(k) clearance K000159 for AGFA DIAGNOSTIC CENTER ADC, ADC COMPACT, AND ADC SOLO, Substantially Equivalent on 2000-02-16. Applicant: Agfa Corp.. Device class: 2.

Clearance details

Applicant: Agfa Corp.
Product code: Code IXK
Device class: Class 2
Regulation: 21 CFR 892.1630
Advisory panel: Radiology
Date received: 2000-01-19
Decision date: 2000-02-16
Decision: Substantially Equivalent
Clearance type: Special
Location: Greenville, SC, US

Download summary PDF View on FDA.gov ↗

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