# Heart Technology, Inc.

- Location (FDA's records): Bellevue, WA
- FDA decisions: 4 (1990–1993): 4 510(k) clearances
- Product codes: MCW (3), DQX (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 9 (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
- Boston Scientific Corp: 3 (https://510kreport.com/company/boston-scientific)
- Cardiovascular Systems, Inc.: 2 (https://510kreport.com/company/cardiovascular-systems)
- Spectranetics Corp.: 2 (https://510kreport.com/company/spectranetics)
- Pathway Medical Technologies, Inc.: 1 (https://510kreport.com/company/pathway-medical-technologies)
- Rex Medical: 1 (https://510kreport.com/company/rex-medical)

## Its most-cited devices
- K901206: Rotablator (1990), cited by 6
- K933238: Rotablator, Modification (1993), cited by 2
- K913450: Heart Technology Rotablator Wireclip (1991), cited by 1

## Recent decisions
- K933238: Rotablator, Modification (Aug 24, 1993)
- K914581: Heart Technology Wireclip (Jan 6, 1992)
- K913450: Heart Technology Rotablator Wireclip (Sep 6, 1991)
- K901206: Rotablator (Sep 14, 1990)

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