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FDA 510(k)

MAGNITUDE 3150M MRI PATIENT MONITOR, MODEL 3150M

K-Number: K040915 · 2004-09-22

ApplicantInvivo Research, Inc.
Decision Date2004-09-22
Product CodeMWI
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MAGNITUDE 3150M MRI PATIENT MONITOR, MODEL 3150M is the device name listed in this FDA 510(k) record. The listed applicant is Invivo Research, Inc.. It received FDA 510(k) clearance on 2004-09-22 under 510(k) number K040915. The device is classified under product code MWI. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MAGNITUDE 3150M MRI PATIENT MONITOR, MODEL 3150M?

MAGNITUDE 3150M MRI PATIENT MONITOR, MODEL 3150M is a medical device that received FDA 510(k) clearance on 2004-09-22. The listed applicant is Invivo Research, Inc.. The 510(k) number is K040915.

When did MAGNITUDE 3150M MRI PATIENT MONITOR, MODEL 3150M receive FDA 510(k) clearance?

MAGNITUDE 3150M MRI PATIENT MONITOR, MODEL 3150M received FDA 510(k) clearance on 2004-09-22, under 510(k) number K040915.

Who is the listed applicant for MAGNITUDE 3150M MRI PATIENT MONITOR, MODEL 3150M?

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

What is the FDA product code for MAGNITUDE 3150M MRI PATIENT MONITOR, MODEL 3150M?

The FDA product code for MAGNITUDE 3150M MRI PATIENT MONITOR, MODEL 3150M is MWI.

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Related Devices (Code: MWI)

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.

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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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