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FDA 510(k)

CMI MAGNETOCARDIOGRAPH

K-Number: K033488 · 2004-07-07

ApplicantCmi Cardiomag Imaging, Inc.
Decision Date2004-07-07
Product CodeDPS
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

CMI MAGNETOCARDIOGRAPH is the device name listed in this FDA 510(k) record. The listed applicant is Cmi Cardiomag Imaging, Inc.. It received FDA 510(k) clearance on 2004-07-07 under 510(k) number K033488. The device is classified under product code DPS. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CMI MAGNETOCARDIOGRAPH?

CMI MAGNETOCARDIOGRAPH is a medical device that received FDA 510(k) clearance on 2004-07-07. The listed applicant is Cmi Cardiomag Imaging, Inc.. The 510(k) number is K033488.

When did CMI MAGNETOCARDIOGRAPH receive FDA 510(k) clearance?

CMI MAGNETOCARDIOGRAPH received FDA 510(k) clearance on 2004-07-07, under 510(k) number K033488.

Who is the listed applicant for CMI MAGNETOCARDIOGRAPH?

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

What is the FDA product code for CMI MAGNETOCARDIOGRAPH?

The FDA product code for CMI MAGNETOCARDIOGRAPH is DPS.

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Related Devices (Code: DPS)

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

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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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