# Biotronik Sales, Inc.

- Location (FDA's records): Mchenry, IL
- FDA decisions: 41 (1980–1988): 41 510(k) clearances
- Product codes: DXY (22), DTB (15), DTD (2), DTE (1), KRG (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
- Biotronik, Inc.: 1 (https://510kreport.com/company/biotronik)

## Its most-cited devices
- K841451: Biotronik DY-Unipolar (1985), cited by 1

## Recent decisions
- K875199: NP Bipolar Endocardial Lead W/VS-1 Connector (Feb 18, 1988)
- K853194: ERA-20 (Mar 11, 1987)
- K860036: Edp-20 Pacemaker (Jan 12, 1987)
- K863878: Trios-M VS-1 Pulse Generator (Dec 10, 1986)
- K863879: Neos-M VS-1 Pulse Generator (Dec 10, 1986)
- K863480: Biotronik Permanent Pacemaker Electrode (Sep 23, 1986)
- K860921: Neos VS-1, Pulse Generator (Aug 8, 1986)
- K860922: Mikros, Mikros VS-1, Pulse Generator (Aug 4, 1986)

Source page: https://510kreport.com/company/biotronik-sales