Omnitron Intl., Inc.
FDA 510(k) & PMA Approved Devices — 7 products
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Total Devices7
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K901615 | PULMOCATH INTRABRONCHIAL CATHETER | JAQ | 1992-11-27 | View |
| 510(k) | K923130 | IR-192 IMPLANT -- MODIFICATION | KXK | 1992-09-21 | View |
| 510(k) | K920431 | OMNITRON NEEDLE APPLICATORS 18 AND 21 GAUGE | JAQ | 1992-05-29 | View |
| 510(k) | K913908 | OMNITRON GYN APPLICATOR SYSTEM | JAQ | 1992-03-06 | View |
| 510(k) | K915253 | IR-192 IMPLANT, MODIFICATION | IWA | 1992-02-27 | View |
| 510(k) | K911775 | OMNICATH IMPLANTED CATHETER AND DEPOT | KXK | 1991-05-08 | View |
| 510(k) | K881665 | OMNITRON REMOTE CONTROLLED RADIONUCLIDE APPLICATOR | JAQ | 1988-08-11 | View |
No matching devices.
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