DeviceClearance

ISA-21 INTERVENTIONAL SPINE ARRAY COIL— 510(k) K021631

Substantially Equivalent

Mri Devices Corp.

FDA 510(k) clearance K021631 for ISA-21 INTERVENTIONAL SPINE ARRAY COIL, Substantially Equivalent on 2002-08-13. Applicant: Mri Devices Corp..

Clearance details

Applicant
Mri Devices Corp.
Product code
Code MOS
Advisory panel
Radiology
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Waukesha, WI, US
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