DILON 2000, MODEL 2000-6X8 AND DILON 2000, MODEL 2000-5X5— 510(k) K984466

Name: FDA 510(k) clearance K984466
Creator: U.S. Food and Drug Administration
Published: 1999-03-16

Substantially Equivalent

Dilon Technologies, Inc.

FDA 510(k) clearance K984466 for DILON 2000, MODEL 2000-6X8 AND DILON 2000, MODEL 2000-5X5, Substantially Equivalent on 1999-03-16. Applicant: Dilon Technologies, Inc.. Device class: 1.

Clearance details

Applicant: Dilon Technologies, Inc.
Product code: Code IYX
Device class: Class 1
Regulation: 21 CFR 892.1100
Advisory panel: Radiology
Date received: 1998-12-16
Decision date: 1999-03-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Newport News, VA, US

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