KONICA DIRECT DIGITIZER, MODEL DD-341— 510(k) K990359

Name: FDA 510(k) clearance K990359
Creator: U.S. Food and Drug Administration
Published: 1999-08-17

Substantially Equivalent

Konica Corp.

FDA 510(k) clearance K990359 for KONICA DIRECT DIGITIZER, MODEL DD-341, Substantially Equivalent on 1999-08-17. Applicant: Konica Corp.. Device class: 2.

Clearance details

Applicant: Konica Corp.
Product code: Code MQB
Device class: Class 2
Regulation: 21 CFR 892.1680
Advisory panel: Radiology
Date received: 1999-02-05
Decision date: 1999-08-17
Decision: Substantially Equivalent
Clearance type: Traditional
Location: New York, NY, US

Download summary PDF View on FDA.gov ↗

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