# American Pacemaker Corp.

- Location (FDA's records): Mchenry, IL
- FDA decisions: 14 (1977–1982): 14 510(k) clearances
- Product codes: DXY (7), DTB (6), DTE (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 1 (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
- Paladin Medical, Inc.: 1 (https://510kreport.com/company/paladin-medical)

## Its most-cited devices
- K821791: External Pulse Generator - EV4542 (1982), cited by 1

## Recent decisions
- K821791: External Pulse Generator - EV4542 (Jul 6, 1982)
- K812807: Apc Implantable Pacing Leads (Jan 18, 1982)
- K812830: Apc Implantable Pacing Lead (Jan 18, 1982)
- K810396: Apc Implantable Pacing Lead, Tined #3262 (May 15, 1981)
- K810397: Apc Implantable Pacing Lead-Flange #3260 (May 15, 1981)
- K810398: Apc Implantable Pacing Lead, Model 3266 (May 15, 1981)
- K810399: Apc Implantabel Pacing Lead, Model 3264 (May 15, 1981)
- K810121: Unifocal 3 (Feb 23, 1981)

Source page: https://510kreport.com/company/american-pacemaker