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FDA 510(k)

MAGNAVIEW M.R.I. VERSIONS 110FH & 110FM W/CARDIAC

K-Number: K896309 · 1990-01-12

ApplicantInstrumentarium Imaging, Inc.
Decision Date1990-01-12
Product CodeLNH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MAGNAVIEW M.R.I. VERSIONS 110FH & 110FM W/CARDIAC 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 1990-01-12 under 510(k) number K896309. 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 MAGNAVIEW M.R.I. VERSIONS 110FH & 110FM W/CARDIAC?

MAGNAVIEW M.R.I. VERSIONS 110FH & 110FM W/CARDIAC is a medical device that received FDA 510(k) clearance on 1990-01-12. The listed applicant is Instrumentarium Imaging, Inc.. The 510(k) number is K896309.

When did MAGNAVIEW M.R.I. VERSIONS 110FH & 110FM W/CARDIAC receive FDA 510(k) clearance?

MAGNAVIEW M.R.I. VERSIONS 110FH & 110FM W/CARDIAC received FDA 510(k) clearance on 1990-01-12, under 510(k) number K896309.

Who is the listed applicant for MAGNAVIEW M.R.I. VERSIONS 110FH & 110FM W/CARDIAC?

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 MAGNAVIEW M.R.I. VERSIONS 110FH & 110FM W/CARDIAC?

The FDA product code for MAGNAVIEW M.R.I. VERSIONS 110FH & 110FM W/CARDIAC is LNH.

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Official Source

View on FDA Database →

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