Intensive Technology, Inc.
FDA 510(k) & PMA Approved Devices — 12 products
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Total Devices12
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K922970 | INTRA-OPERATIVE TEC ATHERECTOMY SYSTEM | MCW | 1993-01-13 | View |
| 510(k) | K912664 | TEC ROTATING DUAL HEMOVALVE | DYB | 1992-08-24 | View |
| 510(k) | K911869 | IVT GUIDING CATHETER | DQY | 1991-10-16 | View |
| 510(k) | K903463 | IVT INTRODUCER SHEATH | DYB | 1991-01-03 | View |
| 510(k) | K904003 | HEMOCHRON(R) HEPARIN RESPONSE TEST | KFF | 1990-11-29 | View |
| 510(k) | K901767 | MODIFIED IVT PERIPHERAL ATHERECTOMY | LIT | 1990-06-28 | View |
| 510(k) | K896403 | MODIFIED IVT PERIPHERAL ATHERECTOMY SYSTEM | LIT | 1990-03-06 | View |
| 510(k) | K895903 | IVT 0.014 GUIDE WIRE | DQX | 1990-01-04 | View |
| 510(k) | K892209 | APTT BY HEMOCHRON(R) | GFO | 1989-06-22 | View |
| 510(k) | K890515 | PERIPHERAL ATHERECTOMY SYSTEM | DWX | 1989-05-23 | View |
| 510(k) | K882804 | 0.014 PERIPHERAL GUIDE WIRE | DQX | 1988-10-28 | View |
| 510(k) | K810107 | RESPA-TROL | JJS | 1981-01-26 | View |
No matching devices.
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