KONICA LASER IMAGER, DRYPRO MODEL 751/752— 510(k) K013052

Name: FDA 510(k) clearance K013052
Creator: U.S. Food and Drug Administration
Published: 2002-01-16

Substantially Equivalent

Konica Minolta Medical & Graphic, Inc.

FDA 510(k) clearance K013052 for KONICA LASER IMAGER, DRYPRO MODEL 751/752, Substantially Equivalent on 2002-01-16. 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: 2001-09-11
Decision date: 2002-01-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Hachioji-Shi Tokyo, JP

Download summary PDF View on FDA.gov ↗

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