Interventional Therapeutics Corp.
FDA 510(k) & PMA Approved Devices — 28 products
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Total Devices28
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K960832 | OCCLUSION BALLOON CATHETER | MJN | 1996-05-29 | View |
| 510(k) | K950398 | CATHETER, BALLOON TYPE | DQO | 1995-10-05 | View |
| 510(k) | K945588 | DISPOSABLE 1CC SYRINGE WITH LUER LOCK | FMF | 1995-02-10 | View |
| 510(k) | K944354 | CONTOUR EMBOLI | HCG | 1994-12-13 | View |
| 510(k) | K930456 | INTHERM SINGLE-STICK RADIALLY EXPANDING DILATOR | KNT | 1993-11-17 | View |
| 510(k) | K914866 | ITC CONTOUR EMBOLI, MODIFICATION | HCG | 1993-11-09 | View |
| 510(k) | K931025 | INTHERM STASIS VALVE SYSTEM | FGE | 1993-09-28 | View |
| 510(k) | K931278 | INTHERM SINGLE-STICK RADIALLY EXPANDING DILATOR | GCJ | 1993-07-23 | View |
| 510(k) | K922609 | ITC CATHETERS W/ HYDROMER | DQY | 1993-04-30 | View |
| 510(k) | K925876 | ITC BUNJI PLATINUM EMBOLIZATION COIL | HCG | 1993-04-15 | View |
| 510(k) | K925523 | ITC BUNJI PLATINUM EMBOLIZATION COIL | HCG | 1993-03-23 | View |
| 510(k) | K922101 | ANGIOGRAPHIC CATHETER -- MODIFICATION | DQO | 1993-02-12 | View |
| 510(k) | K923518 | GUIDING CATHETER | DQY | 1993-01-12 | View |
| 510(k) | K924451 | INTHERM SINGLE-STICK RADIALLY EXPANDING DILATOR | FGE | 1992-10-23 | View |
| 510(k) | K921399 | OCCLUSION BALLON CATHETER MODIFICAION | DXC | 1992-09-25 | View |
| 510(k) | K920324 | ITC BUNJI COIL (MODIFICATION) | HCG | 1992-07-29 | View |
| 510(k) | K915625 | INTRODUCER CATHETER | DYB | 1992-06-03 | View |
| 510(k) | K912532 | ITC HIESHIMA TAPER SELECT(TM) PERCUTANEOUS CATH | DQO | 1991-12-11 | View |
| 510(k) | K913052 | ITC GUIDING CATHETER | DQY | 1991-11-22 | View |
| 510(k) | K913932 | PERCUTANEOUS DILATOR WITH SHEATH | FGE | 1991-11-22 | View |
No matching devices.
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