FLEXART QD HEAD/NECK COIL— 510(k) K961391

Substantially Equivalent

Toshiba America Mri, Inc.

FDA 510(k) clearance K961391 for FLEXART QD HEAD/NECK COIL, Substantially Equivalent on 1996-07-09. Applicant: Toshiba America Mri, Inc..

Clearance details

Applicant: Toshiba America Mri, Inc.
Product code: Code MOS
Advisory panel: Radiology
Date received: 1996-04-10
Decision date: 1996-07-09
Decision: Substantially Equivalent
Clearance type: Traditional
Location: S. San Francisco, CA, US

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