FDA 510(k) Applications Submitted by GUY GANSEL
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K982225 | 06/24/1998 | SPIRACLE TECHNOLOGY-BI-FLOW DEMAND/RESUSCITATOR VALVE, MODEL 504 | SPIRACLE TECHNOLOGY |
| K973347 | 09/05/1997 | TSX PRM PULMONARY RESUSCITATION MONITOR | SPIRACLE TECHNOLOGY |
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