KONICA KFDR-S— 510(k) K896739

Substantially Equivalent

Konica Medical Corp.

FDA 510(k) clearance K896739 for KONICA KFDR-S, Substantially Equivalent on 1990-04-30. Applicant: Konica Medical Corp..

Clearance details

Applicant: Konica Medical Corp.
Product code: Code LMA
Advisory panel: Radiology
Date received: 1989-11-30
Decision date: 1990-04-30
Decision: Substantially Equivalent
Clearance type: Traditional
Location: New York, NY, US

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