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Revivant Corp.

FDA 510(k) & PMA Approved Devices — 4 products

Total Devices4
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K040453 AUTOPULSE RESUSCITATION SYSTEM, MODEL 100DRM2004-03-11 View
510(k) K032852 MODIFICATION TO: AUTOPULSE RESUSCITATION SYSTEM MODEL 100DRM2003-11-12 View
510(k) K022345 AUTOPULSE RESUSCITATION SYSTEMDRM2002-08-15 View
510(k) K011046 AUTOPULSE, MODEL 100DRM2001-10-25 View
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