# Interventional Therapeutics Corp.

- Location (FDA's records): South San Francisco, CA
- FDA decisions: 28 (1987–1996): 28 510(k) clearances
- Product codes: HCG (7), DQO (4), FGE (4), DQY (3), DYB (2), DYG (1), KNT (1), FMF (1), MJN (1), DXC (1), GCJ (1), DQA (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 14 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Target Therapeutics: 4 (https://510kreport.com/company/target-therapeutics)
- Biosphere Medical, S.A.: 3 (https://510kreport.com/company/biosphere-medical)
- Boston Scientific, Target: 3 (https://510kreport.com/company/boston-scientific-target)
- Boston Scientific Corp: 2 (https://510kreport.com/company/boston-scientific)
- Acta Vascular Systems, Inc.: 1 (https://510kreport.com/company/acta-vascular-systems)
- Cordis Neurovascular, Inc.: 1 (https://510kreport.com/company/cordis-neurovascular)

## Its most-cited devices
- K944354: Contour Emboli (1994), cited by 7
- K871047: Radiopaque Spherical Emboli (Rse) (1987), cited by 4
- K960832: Occlusion Balloon Catheter (1996), cited by 1
- K921399: Occlusion Ballon Catheter Modificaion (1992), cited by 1
- K950398: Catheter, Balloon Type (1995), cited by 1

## Recent decisions
- K960832: Occlusion Balloon Catheter (May 29, 1996)
- K950398: Catheter, Balloon Type (Oct 5, 1995)
- K945588: Disposable 1CC Syringe with Luer Lock (Feb 10, 1995)
- K944354: Contour Emboli (Dec 13, 1994)
- K930456: Intherm Single-Stick Radially Expanding Dilator (Nov 17, 1993)
- K914866: Itc Contour Emboli, Modification (Nov 9, 1993)
- K931025: Intherm Stasis Valve System (Sep 28, 1993)
- K931278: Intherm Single-Stick Radially Expanding Dilator (Jul 23, 1993)

Source page: https://510kreport.com/company/interventional-therapeutics