# Prucka Engineering, Inc.

- Location (FDA's records): Houston, TX
- FDA decisions: 6 (1989–2000): 6 510(k) clearances
- Product codes: DRF (2), DPS (2), DRR (1), DQK (1)
- Predicates its devices cite: 3 (0 its own); citations of its devices by later devices: 5 (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 whose devices it cites most
- Quinton Electrophysiology Corp.: 1 (https://510kreport.com/company/quinton-electrophysiology)
- Electrophysiology Systems, Inc.: 1 (https://510kreport.com/company/electrophysiology-systems)
- Biosense, Ltd.: 1 (https://510kreport.com/company/biosense)

## Firms that cite its devices most
- Quinton Electrophysiology Corp.: 2 (https://510kreport.com/company/quinton-electrophysiology)
- Mennen Medical, Inc.: 1 (https://510kreport.com/company/mennen-medical)
- Cathdata, Inc.: 1 (https://510kreport.com/company/cathdata)
- Siemens Medical Systems, Inc.: 1 (https://510kreport.com/company/siemens-medical-systems)

## Its most-cited devices
- K902716: PE Electrophysiology Lab System (Peep) (1990), cited by 2
- K993414: Prucka Engineering Inc. Cardiolab EP System,Version 4.2 (2000), cited by 2
- K910307: Cardiolab Amplifier Module (Cam) (1991), cited by 1

## Recent decisions
- K993414: Prucka Engineering Inc. Cardiolab EP System,Version 4.2 (Apr 7, 2000)
- K960321: Cardiocath Catheterization Lab System (Aug 21, 1996)
- K904747: Pei Plaque Electrode Array (Oct 9, 1991)
- K910307: Cardiolab Amplifier Module (Cam) (Apr 12, 1991)
- K902716: PE Electrophysiology Lab System (Peep) (Sep 4, 1990)
- K895916: PE Intercardiac Mapping System (Icms) (Dec 13, 1989)

Source page: https://510kreport.com/company/prucka-engineering