Medi-Globe Corporation
FDA 510(k) & PMA Approved Devices — 5 products
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Total Devices5
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K153264 | EasyPass Guidewire | OCY | 2016-05-19 | View |
| 510(k) | K091257 | MEDI-GLOBE SONOTIP II EBUS-TBNA NEEDLE SYSTEM | FCG | 2009-05-08 | View |
| 510(k) | K083802 | SONOTIP II 25-GAUGE ULTRASOUND NEEDLE SYSTEM, MODELS GUS-01-18-025 AND GUS-01-27-025 | FCG | 2009-03-20 | View |
| 510(k) | K070129 | SONOTIP II ULTRASOUND NEEDLE SYSTEM | FCG | 2007-01-31 | View |
| 510(k) | K061684 | MEDI-GLOBE ROTA-CUT SPHINCTEROTOME | KNS | 2006-06-27 | View |
No matching devices.
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