FDA 510(k) Applications Submitted by GENERAL MEDITECH, INC.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K082789 | 09/23/2008 | G1B PULSE OXIMETER | GENERAL MEDITECH, INC. |
| K092970 | 09/25/2009 | GENERAL PATIENT MONITORS, MODELS: G3C/ G3D/ G3F/ G3G/ G3H | GENERAL MEDITECH, INC. |
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