General Meditech, Inc.
FDA 510(k) & PMA Approved Devices — 2 products
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Total Devices2
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K092970 | GENERAL PATIENT MONITORS, MODELS: G3C/ G3D/ G3F/ G3G/ G3H | MHX | 2010-02-02 | View |
| 510(k) | K082789 | G1B PULSE OXIMETER | DQA | 2009-01-07 | View |
No matching devices.
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