# Intervascular, Inc.

- Location (FDA's records): Clearwater, FL
- FDA decisions: 20 (1984–2011): 20 510(k) clearances
- Names in FDA's records: Intervascular, Inc. (16); Intervascular (3); Intervascular Sas (1)
- Product codes: DSY (17), DXZ (2), DWF (1)
- Predicates its devices cite: 1 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 5 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Meadox Medicals, Div. Boston Scientific Corp.: 1 (https://510kreport.com/company/meadox-medicals-div-boston-scientific)

## Recent decisions
- K103347: Cardioroot Woven Collagen Coated Vascular Prostheses (Feb 2, 2011)
- K042984: Intergard Woven Connector Graft, Model IGW0030-10C (Feb 18, 2005)
- K022242: Intervascular Intergard Knitted Vascular Graft Sizer (Aug 14, 2002)
- K013651: Intergard Hemabridge Collagen Coated Vascular Prosthesis, Intergard Aortic Arch Collagen Coated Vascular Prosthesis (Feb 27, 2002)
- K990800: Intergard Knitted Ultra Thin and Intergard Knitted Collagen Coated and Heparin Bonded Vascular Prothesis (Jan 8, 2001)
- K984294: Modification of Intergard Woven Collagen Coated Vascular Prostheses (Feb 22, 1999)
- K983819: Intergard Knitted Ultra Thin Collagen Coated Vascular Graft and Hemacarotid Patch Ultra Thin (Nov 24, 1998)
- K970843: Intergard Woven Collagen Coated Vascular Prostheses (Jun 5, 1997)

Source page: https://510kreport.com/company/intervascular