Intensive Technology, Inc.
FDA 510(k) medical device clearances.
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.