# Cardiac Pacemakers, Inc.

- Location (FDA's records): Mchenry, IL
- FDA decisions: 76 (1977–2010): 76 510(k) clearances
- Product codes: DXY (37), FRN (8), KRG (7), DTD (5), DWS (2), DQY (2), DXH (2), DRB (2), DTA (1), FMF (1), DRR (1), FPA (1)
- Predicates its devices cite: 2 (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 whose devices it cites most
- Guidant Corp.: 2 (https://510kreport.com/company/guidant)

## Firms that cite its devices most
- Guidant Corp.: 5 (https://510kreport.com/company/guidant)
- Boston Scientific Corp: 2 (https://510kreport.com/company/boston-scientific)

## Its most-cited devices
- K905674: Lead Stylet (1991), cited by 4
- K093969: Acuity Break-Away Guide Catheter (2010), cited by 2
- K843060: Sentra (1984), cited by 1

## Recent decisions
- K093969: Acuity Break-Away Guide Catheter (Mar 5, 2010)
- K080154: Acuity Universal Cutter (Mar 20, 2008)
- K934727: Replacement Parts for Cpi 6888 Lead Tunneler (Jan 10, 1994)
- K920601: Astra T2, Astra T4, Astra T6 (Oct 28, 1992)
- K912379: PDT Carryall Transmitter, Various Models (Jun 17, 1991)
- K905674: Lead Stylet (Jan 30, 1991)
- K900498: Modified Betatron IV Insulin Infusion System (Feb 23, 1990)
- K894738: Model 6888 Lead Tunneler (Sep 13, 1989)

Source page: https://510kreport.com/company/cardiac-pacemakers