KONICA LASER IMAGER, DRYPRO MODEL 722— 510(k) K992586

Name: FDA 510(k) clearance K992586
Creator: U.S. Food and Drug Administration
Published: 1999-10-29

Substantially Equivalent

Konica Corp.

FDA 510(k) clearance K992586 for KONICA LASER IMAGER, DRYPRO MODEL 722, Substantially Equivalent on 1999-10-29. Applicant: Konica Corp.. Device class: 2.

Clearance details

Applicant: Konica Corp.
Product code: Code LMC
Device class: Class 2
Regulation: 21 CFR 892.2040
Advisory panel: Radiology
Date received: 1999-08-02
Decision date: 1999-10-29
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mie-Ken, JP

Download summary PDF View on FDA.gov ↗

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