# Intensive Technology, Inc.

- Location (FDA's records): San Diego, CA
- FDA decisions: 13 (1981–1993): 12 510(k) clearances and 1 original PMA approval
- Product codes: DQX (2), DYB (2), LIT (2), MCX (1), JJS (1), GFO (1), DWX (1), KFF (1), MCW (1), DQY (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 7 (0 its own)
- Recalls linked to its devices: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Boston Scientific /International Technologies: 5 (https://510kreport.com/company/boston-scientific-international-technologies)
- Pathway Medical Technologies, Inc.: 2 (https://510kreport.com/company/pathway-medical-technologies)

## Its most-cited devices
- K882804: 0.014 Peripheral Guide Wire (1988), cited by 2
- K895903: Ivt 0.014 Guide Wire (1990), cited by 2
- K890515: Peripheral Atherectomy System (1989), cited by 1
- K922970: Intra-Operative Tec Atherectomy System (1993), cited by 1
- K911869: Ivt Guiding Catheter (1991), cited by 1

## Recent decisions
- P910019: Ivt Coronary Atherectomy System (Tec)(R) (May 18, 1993)
- K922970: Intra-Operative Tec Atherectomy System (Jan 13, 1993)
- K912664: Tec Rotating Dual Hemovalve (Aug 24, 1992)
- K911869: Ivt Guiding Catheter (Oct 16, 1991)
- K903463: Ivt Introducer Sheath (Jan 3, 1991)
- K904003: Hemochron (R) Heparin Response Test (Nov 29, 1990)
- K901767: Modified Ivt Peripheral Atherectomy (Jun 28, 1990)
- K896403: Modified Ivt Peripheral Atherectomy System (Mar 6, 1990)

Source page: https://510kreport.com/company/intensive-technology