DRY LASER IMAGER, DRYPRO MODEL 832— 510(k) K061999

Substantially Equivalent

Konica Minolta Medical & Graphic, Inc.

FDA 510(k) clearance K061999 for DRY LASER IMAGER, DRYPRO MODEL 832, Substantially Equivalent on 2006-08-15. Applicant: Konica Minolta Medical & Graphic, Inc..

Clearance details

Applicant: Konica Minolta Medical & Graphic, Inc.
Product code: Code LMC
Advisory panel: Radiology
Date received: 2006-07-14
Decision date: 2006-08-15
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Hachioji-Shi, JP

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