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FDA 510(k)

KINEMATIC MRI MOVIEMAKER

K-Number: K924154 · 1992-11-23

ApplicantResonex, Inc.
Decision Date1992-11-23
Product CodeLNH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

KINEMATIC MRI MOVIEMAKER is the device name listed in this FDA 510(k) record. The listed applicant is Resonex, Inc.. It received FDA 510(k) clearance on 1992-11-23 under 510(k) number K924154. 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 KINEMATIC MRI MOVIEMAKER?

KINEMATIC MRI MOVIEMAKER is a medical device that received FDA 510(k) clearance on 1992-11-23. The listed applicant is Resonex, Inc.. The 510(k) number is K924154.

When did KINEMATIC MRI MOVIEMAKER receive FDA 510(k) clearance?

KINEMATIC MRI MOVIEMAKER received FDA 510(k) clearance on 1992-11-23, under 510(k) number K924154.

Who is the listed applicant for KINEMATIC MRI MOVIEMAKER?

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

What is the FDA product code for KINEMATIC MRI MOVIEMAKER?

The FDA product code for KINEMATIC MRI MOVIEMAKER is LNH.

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Other records listing Resonex, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K935369FAST SPIN ECHO (FSE)K935570NOISE FILTER FOR PARADIGM MAGNETIC RESONANCE IMAGING SYSTEMK931392ECG GATING UNITK9238703DTOF MRAK9238233D IMAGINGK922677MAGNETIZATION TRANSFER CONTRAST

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Related Devices (Code: 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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