AIRIS MAGNETIC RESONANCE DIAGNOSTIC DEVICE— 510(k) K980691

Substantially Equivalent

Hitachi Medical Systems America, Inc.

FDA 510(k) clearance K980691 for AIRIS MAGNETIC RESONANCE DIAGNOSTIC DEVICE, Substantially Equivalent on 1998-05-11. Applicant: Hitachi Medical Systems America, Inc..

Clearance details

Applicant: Hitachi Medical Systems America, Inc.
Product code: Code MOS
Advisory panel: Radiology
Date received: 1998-02-23
Decision date: 1998-05-11
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Twinsburg, OH, US

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