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FDA 510(k), K033488, CMI MAGNETOCARDIOGRAPH
FDA 510(k), K033488, CMI MAGNETOCARDIOGRAPH
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510(K) Number: K033488
Device Name: CMI MAGNETOCARDIOGRAPH
Manufacturer: CMI CARDIOMAG IMAGING INC
Device Classification Name: electrocardiograph
Regulation Number: 870.2340
Classification Product Code: DPS
Date Received: 11/04/2003
Decision Date: 07/07/2004
Regulation Medical Specialty: Cardiovascular
Device Name: CMI MAGNETOCARDIOGRAPH
Manufacturer: CMI CARDIOMAG IMAGING INC
Device Classification Name: electrocardiograph
Regulation Number: 870.2340
Classification Product Code: DPS
Date Received: 11/04/2003
Decision Date: 07/07/2004
Regulation Medical Specialty: Cardiovascular
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks
NOTE: This document is not currently in our library. Upon purchase, we will request the document from the FDA FOIA office. Learn more about Fast-Track Requests here.
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