KONICA LASER IMAGER, MODEL DRYPRO MODEL 771— 510(k) K032681

Name: FDA 510(k) clearance K032681
Creator: U.S. Food and Drug Administration
Published: 2003-09-24

Substantially Equivalent

Konica Medical and Graphic Corporation

FDA 510(k) clearance K032681 for KONICA LASER IMAGER, MODEL DRYPRO MODEL 771, Substantially Equivalent on 2003-09-24. Applicant: Konica Medical and Graphic Corporation. Device class: 2.

Clearance details

Applicant: Konica Medical and Graphic Corporation
Product code: Code LMC
Device class: Class 2
Regulation: 21 CFR 892.2040
Advisory panel: Radiology
Date received: 2003-08-29
Decision date: 2003-09-24
Decision: Substantially Equivalent
Clearance type: Special
Location: Mie-Ken, JP

Download summary PDF View on FDA.gov ↗

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