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FDA 510(k), K150564, Spaulding Electrocardiograph 2100iQ
FDA 510(k), K150564, Spaulding Electrocardiograph 2100iQ
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$149.00 USD
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510(K) Number: K150564
Device Name: Spaulding Electrocardiograph 2100iQ
Manufacturer: Spaulding Clinical Research, LLC
Device Classification Name: electrocardiograph
Regulation Number: 870.2340
Classification Product Code: DPS
Date Received: 03/06/2015
Decision Date: 08/12/2015
Regulation Medical Specialty: Cardiovascular
Device Name: Spaulding Electrocardiograph 2100iQ
Manufacturer: Spaulding Clinical Research, LLC
Device Classification Name: electrocardiograph
Regulation Number: 870.2340
Classification Product Code: DPS
Date Received: 03/06/2015
Decision Date: 08/12/2015
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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