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FDA 510(k)

MEGA 4 MAGNETIC RESONANCE IMAGING SYSTEM

K-Number: K902044 · 1990-08-23

ApplicantInstrumentarium Imaging, Inc.
Decision Date1990-08-23
Product CodeLNH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MEGA 4 MAGNETIC RESONANCE IMAGING SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Instrumentarium Imaging, Inc.. It received FDA 510(k) clearance on 1990-08-23 under 510(k) number K902044. 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 MEGA 4 MAGNETIC RESONANCE IMAGING SYSTEM?

MEGA 4 MAGNETIC RESONANCE IMAGING SYSTEM is a medical device that received FDA 510(k) clearance on 1990-08-23. The listed applicant is Instrumentarium Imaging, Inc.. The 510(k) number is K902044.

When did MEGA 4 MAGNETIC RESONANCE IMAGING SYSTEM receive FDA 510(k) clearance?

MEGA 4 MAGNETIC RESONANCE IMAGING SYSTEM received FDA 510(k) clearance on 1990-08-23, under 510(k) number K902044.

Who is the listed applicant for MEGA 4 MAGNETIC RESONANCE IMAGING SYSTEM?

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

What is the FDA product code for MEGA 4 MAGNETIC RESONANCE IMAGING SYSTEM?

The FDA product code for MEGA 4 MAGNETIC RESONANCE IMAGING SYSTEM is LNH.

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Official Source

View on FDA Database →

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

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