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FDA 510(k)

OPEN MAGNETIC RESONANCE IMAGING SYSTEM, MODEL MPF3000-III

K-Number: K091669 · 2009-06-18

ApplicantXioao Mdt Technology Co, Ltd.
Decision Date2009-06-18
Product CodeLNH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

OPEN MAGNETIC RESONANCE IMAGING SYSTEM, MODEL MPF3000-III is the device name listed in this FDA 510(k) record. The listed applicant is Xioao Mdt Technology Co, Ltd.. It received FDA 510(k) clearance on 2009-06-18 under 510(k) number K091669. The device is classified under product code LNH. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the OPEN MAGNETIC RESONANCE IMAGING SYSTEM, MODEL MPF3000-III?

OPEN MAGNETIC RESONANCE IMAGING SYSTEM, MODEL MPF3000-III is a medical device that received FDA 510(k) clearance on 2009-06-18. The listed applicant is Xioao Mdt Technology Co, Ltd.. The 510(k) number is K091669.

When did OPEN MAGNETIC RESONANCE IMAGING SYSTEM, MODEL MPF3000-III receive FDA 510(k) clearance?

OPEN MAGNETIC RESONANCE IMAGING SYSTEM, MODEL MPF3000-III received FDA 510(k) clearance on 2009-06-18, under 510(k) number K091669.

Who is the listed applicant for OPEN MAGNETIC RESONANCE IMAGING SYSTEM, MODEL MPF3000-III?

The FDA 510(k) record lists Xioao Mdt Technology Co, Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for OPEN MAGNETIC RESONANCE IMAGING SYSTEM, MODEL MPF3000-III?

The FDA product code for OPEN MAGNETIC RESONANCE IMAGING SYSTEM, MODEL MPF3000-III is LNH.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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