LASER IMAGER DRYPRO MODEL 873— 510(k) K081637

Name: FDA 510(k) clearance K081637
Creator: U.S. Food and Drug Administration
Published: 2008-07-01

Substantially Equivalent

Konica Minolta Medical & Graphic, Inc.

FDA 510(k) clearance K081637 for LASER IMAGER DRYPRO MODEL 873, Substantially Equivalent on 2008-07-01. Applicant: Konica Minolta Medical & Graphic, Inc.. Device class: 2.

Clearance details

Applicant: Konica Minolta Medical & Graphic, Inc.
Product code: Code LMC
Device class: Class 2
Regulation: 21 CFR 892.2040
Advisory panel: Radiology
Date received: 2008-06-11
Decision date: 2008-07-01
Decision: Substantially Equivalent
Clearance type: Special
Location: New York, NY, US

Download summary PDF View on FDA.gov ↗

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