Oldelft Corp. of America
FDA 510(k) & PMA Approved Devices — 9 products
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Total Devices9
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K980296 | OLDELFT DIGIDELCA | KPR | 1998-04-17 | View |
| 510(k) | K973219 | AMBER DU | KPR | 1997-10-08 | View |
| 510(k) | K946128 | SIMULIX-HP | KPQ | 1995-05-12 | View |
| 510(k) | K950037 | N 800 HF | IZO | 1995-02-15 | View |
| 510(k) | K932848 | SIMULIX-MC CT EXTENSION | JAK | 1994-03-22 | View |
| 510(k) | K923584 | THERAPAX DXT 300 SERIES 3 | JAD | 1993-01-15 | View |
| 510(k) | K914784 | PAPILLION PROCTOSCOPE | KQA | 1992-06-05 | View |
| 510(k) | K912466 | OLDELFT SIMULIX-MC | KPQ | 1991-06-28 | View |
| 510(k) | K892659 | ELECTRODELCA | IZG | 1989-11-21 | View |
No matching devices.
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