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FDA 510(k)

MRI SYSTEM, MODEL MAGFINDER II / AI 3200

K-Number: K072850 · 2007-11-21

ApplicantAdvanced Imaging Laboratory
Decision Date2007-11-21
Product CodeLNH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MRI SYSTEM, MODEL MAGFINDER II / AI 3200 is the device name listed in this FDA 510(k) record. The listed applicant is Advanced Imaging Laboratory. It received FDA 510(k) clearance on 2007-11-21 under 510(k) number K072850. 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 MRI SYSTEM, MODEL MAGFINDER II / AI 3200?

MRI SYSTEM, MODEL MAGFINDER II / AI 3200 is a medical device that received FDA 510(k) clearance on 2007-11-21. The listed applicant is Advanced Imaging Laboratory. The 510(k) number is K072850.

When did MRI SYSTEM, MODEL MAGFINDER II / AI 3200 receive FDA 510(k) clearance?

MRI SYSTEM, MODEL MAGFINDER II / AI 3200 received FDA 510(k) clearance on 2007-11-21, under 510(k) number K072850.

Who is the listed applicant for MRI SYSTEM, MODEL MAGFINDER II / AI 3200?

The FDA 510(k) record lists Advanced Imaging Laboratory as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MRI SYSTEM, MODEL MAGFINDER II / AI 3200?

The FDA product code for MRI SYSTEM, MODEL MAGFINDER II / AI 3200 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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