DuoFLEX Coil Suite— 510(k) K173290

Substantially Equivalent

Mr Instruments, Inc.

FDA 510(k) clearance K173290 for DuoFLEX Coil Suite, Substantially Equivalent on 2017-11-28. Applicant: Mr Instruments, Inc..

Clearance details

Applicant: Mr Instruments, Inc.
Product code: Code MOS
Advisory panel: Radiology
Date received: 2017-10-16
Decision date: 2017-11-28
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Minnetonka, MN, US

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