FDA 510(k), K040453, AUTOPULSE RESUSCITATION SYSTEM, MODEL 100
FDA 510(k), K040453, AUTOPULSE RESUSCITATION SYSTEM, MODEL 100
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
Total pages: 68
Fully redacted pages: 10
Content pages: 58
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