FDA 510(k) Applications Submitted by SUSANNE T SMITH
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K022345 | 07/19/2002 | AUTOPULSE RESUSCITATION SYSTEM | REVIVANT CORP. |
| K973789 | 10/06/1997 | NORIAN CRANIAL REPAIR SYSTEM (CRS)BONE CEMENT- 5CC KIT, NORIAN CRANIAL REPAIR SYSTEM (CRS) BONE CEMENT- 10CC | NORIAN CORP. |
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