Intensive Technology, Inc.
Intensive Technology, Inc. holds FDA 510(k) medical device clearances, first cleared 1981, most recent 1993.
Top product codes for Intensive Technology, Inc.
Recent clearances by Intensive Technology, Inc.
- K922970 — INTRA-OPERATIVE TEC ATHERECTOMY SYSTEM
- K912664 — TEC ROTATING DUAL HEMOVALVE
- K911869 — IVT GUIDING CATHETER
- K903463 — IVT INTRODUCER SHEATH
- K904003 — HEMOCHRON(R) HEPARIN RESPONSE TEST
- K901767 — MODIFIED IVT PERIPHERAL ATHERECTOMY
- K896403 — MODIFIED IVT PERIPHERAL ATHERECTOMY SYSTEM
- K895903 — IVT 0.014 GUIDE WIRE
- K892209 — APTT BY HEMOCHRON(R)
- K890515 — PERIPHERAL ATHERECTOMY SYSTEM
- K882804 — 0.014 PERIPHERAL GUIDE WIRE
- K810107 — RESPA-TROL
Data sourced from openFDA. This site is unofficial and independent of the FDA.