FDA 510(k) Applications Submitted by TOM KROENKE
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K983684 | 10/20/1998 | DATEX-OHMEDA 3800+/3800P+ OR 3900/3900P PULSE OXIMETERS | DATEX-OHMEDA, INC. |
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