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FDA 510(k)

FIELD EFFECTS MRI SYSTEM

K-Number: K983902 · 1999-01-07

ApplicantIntermagnetics General Corp.
Decision Date1999-01-07
Product CodeLNH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

FIELD EFFECTS MRI SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Intermagnetics General Corp.. It received FDA 510(k) clearance on 1999-01-07 under 510(k) number K983902. 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 FIELD EFFECTS MRI SYSTEM?

FIELD EFFECTS MRI SYSTEM is a medical device that received FDA 510(k) clearance on 1999-01-07. The listed applicant is Intermagnetics General Corp.. The 510(k) number is K983902.

When did FIELD EFFECTS MRI SYSTEM receive FDA 510(k) clearance?

FIELD EFFECTS MRI SYSTEM received FDA 510(k) clearance on 1999-01-07, under 510(k) number K983902.

Who is the listed applicant for FIELD EFFECTS MRI SYSTEM?

The FDA 510(k) record lists Intermagnetics General Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for FIELD EFFECTS MRI SYSTEM?

The FDA product code for FIELD EFFECTS MRI SYSTEM 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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