Intervascular, Inc.
Intervascular, Inc. holds FDA 510(k) medical device clearances, first cleared 1984, most recent 2001.
Top product codes for Intervascular, Inc.
Recent clearances by Intervascular, Inc.
- K990800 — INTERGARD KNITTED ULTRA THIN AND INTERGARD KNITTED COLLAGEN COATED AND HEPARIN BONDED VASCULAR PROTHESIS
- K984294 — MODIFICATION OF INTERGARD WOVEN COLLAGEN COATED VASCULAR PROSTHESES
- K983819 — INTERGARD KNITTED ULTRA THIN COLLAGEN COATED VASCULAR GRAFT AND HEMACAROTID PATCH ULTRA THIN
- K970843 — INTERGARD WOVEN COLLAGEN COATED VASCULAR PROSTHESES
- K964625 — HEMAPATCH VASCULAR PATCHES, INTERGARD AND INTERGARD-RS VASCULAR PROSTHESES
- K921659 — ULTRA LOW POROSITY DACRON WOVEN PATCH
- K913143 — OCHSNER ULP BIFURCATION VASCULAR PROTHESIS
- K912911 — LOW POROSITY (LP) VASCULAR PROSTHESIS
- K905269 — OCHSNER 500 VASCULAR PROSTHESIS
- K905270 — OCHSNER 50 VASCULAR PROSTHESIS
- K903964 — OCHSNER 50 BIFURCATION
- K881508 — OCHSNER & MICRON FABRIC PATCH
- K870884 — RADIALLY-SUPPORTED VASCULAR PROSTHESES
- K862739 — INTERVASCULAR OCHSNER MICRON VASCULAR PROSTHESES
- K854845 — INTERVASCULAROCHSNER 50 AND OCHSNER 500 VASCULAR
- K833716 — LP200 & HP800 SERIES VASCULAR PROSTH
Data sourced from openFDA. This site is unofficial and independent of the FDA.