FDA 510(k) Applications Submitted by DAVE SIMARD
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K001315 | 04/26/2000 | MODIFICATION TO KION ANESTHESIA SYSTEM | SIEMENS ELEMA AB |
| K002137 | 07/14/2000 | CATHCOR DESKTOP | SIEMENS ELEMA AB |
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