Intensive Technology, Inc.
12 FDA 510(k) clearances · Manufacturer
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| Record | Firm | Date |
|---|---|---|
| INTRA-OPERATIVE TEC ATHERECTOMY SYSTEM (K922970) | Intensive Technology, Inc. | 1993-01-13 |
| TEC ROTATING DUAL HEMOVALVE (K912664) | Intensive Technology, Inc. | 1992-08-24 |
| IVT GUIDING CATHETER (K911869) | Intensive Technology, Inc. | 1991-10-16 |
| IVT INTRODUCER SHEATH (K903463) | Intensive Technology, Inc. | 1991-01-03 |
| HEMOCHRON(R) HEPARIN RESPONSE TEST (K904003) | Intensive Technology, Inc. | 1990-11-29 |
| MODIFIED IVT PERIPHERAL ATHERECTOMY (K901767) | Intensive Technology, Inc. | 1990-06-28 |
| MODIFIED IVT PERIPHERAL ATHERECTOMY SYSTEM (K896403) | Intensive Technology, Inc. | 1990-03-06 |
| IVT 0.014 GUIDE WIRE (K895903) | Intensive Technology, Inc. | 1990-01-04 |
| APTT BY HEMOCHRON(R) (K892209) | Intensive Technology, Inc. | 1989-06-22 |
| PERIPHERAL ATHERECTOMY SYSTEM (K890515) | Intensive Technology, Inc. | 1989-05-23 |
| 0.014 PERIPHERAL GUIDE WIRE (K882804) | Intensive Technology, Inc. | 1988-10-28 |
| RESPA-TROL (K810107) | Intensive Technology, Inc. | 1981-01-26 |
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