FDA 510(k) Applications Submitted by REVIVANT CORP.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K011046 | 04/06/2001 | AUTOPULSE, MODEL 100 | REVIVANT CORP. |
| K040453 | 02/23/2004 | AUTOPULSE RESUSCITATION SYSTEM, MODEL 100 | REVIVANT CORP. |
| K032852 | 09/12/2003 | MODIFICATION TO: AUTOPULSE RESUSCITATION SYSTEM MODEL 100 | REVIVANT CORP. |
| K022345 | 07/19/2002 | AUTOPULSE RESUSCITATION SYSTEM | REVIVANT CORP. |
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