ACCURAD-200 SYSTEM & ACCURAD-300 PLUS SYSTEM— 510(k) K925705

Name: FDA 510(k) clearance K925705
Creator: U.S. Food and Drug Administration
Published: 1992-12-28

Substantially Equivalent

Denar Corp.

FDA 510(k) clearance K925705 for ACCURAD-200 SYSTEM & ACCURAD-300 PLUS SYSTEM, Substantially Equivalent on 1992-12-28. Applicant: Denar Corp.. Device class: 1.

Clearance details

Applicant: Denar Corp.
Product code: Code IWY
Device class: Class 1
Regulation: 21 CFR 892.1920
Advisory panel: Radiology
Date received: 1992-11-12
Decision date: 1992-12-28
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Chicago, IL, US

Download summary PDF View on FDA.gov ↗

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