# Heart Technology Mfg., Inc.

- Location (FDA's records): Redmond, WA
- FDA decisions: 3 (1995–1996): 3 510(k) clearances
- Product codes: MCW (3)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 2 (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
- Pathway Medical Technologies, Inc.: 1 (https://510kreport.com/company/pathway-medical-technologies)
- Boston Scientific Corp: 1 (https://510kreport.com/company/boston-scientific)

## Its most-cited devices
- K954604: Rotablator Rotational Angioplasty System Rotablator System's Guide Wire Line; Hti Floppy (1996), cited by 1
- K960379: Rotablator System's Guide Wire Line: Support Rotawire Rail Rota Wire (1996), cited by 1

## Recent decisions
- K960379: Rotablator System's Guide Wire Line: Support Rotawire Rail Rota Wire (Apr 25, 1996)
- K954604: Rotablator Rotational Angioplasty System Rotablator System's Guide Wire Line; Hti Floppy (Jan 18, 1996)
- K953997: Rotablator Rotational Angioplasty (Dec 22, 1995)

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