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FDA 510(k), K040453, AUTOPULSE RESUSCITATION SYSTEM, MODEL 100
FDA 510(k), K040453, AUTOPULSE RESUSCITATION SYSTEM, MODEL 100
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510(K) Number: K040453
Device Name: AUTOPULSE RESUSCITATION SYSTEM, MODEL 100
Manufacturer: REVIVANT CORP.
Device Classification Name: compressor, cardiac, external
Regulation Number: 870.5200
Classification Product Code: DRM
Date Received: 02/23/2004
Decision Date: 03/11/2004
Regulation Medical Specialty: Cardiovascular
Device Name: AUTOPULSE RESUSCITATION SYSTEM, MODEL 100
Manufacturer: REVIVANT CORP.
Device Classification Name: compressor, cardiac, external
Regulation Number: 870.5200
Classification Product Code: DRM
Date Received: 02/23/2004
Decision Date: 03/11/2004
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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