DeviceClearance

HI-RES 9000 PHASED ARRAY CAROTID COIL— 510(k) K001210

Substantially Equivalent

Usa Instruments, Inc.

FDA 510(k) clearance K001210 for HI-RES 9000 PHASED ARRAY CAROTID COIL, Substantially Equivalent on 2000-06-09. Applicant: Usa Instruments, Inc..

Clearance details

Applicant
Usa Instruments, Inc.
Product code
Code MOS
Advisory panel
Radiology
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Aurora, OH, US
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