# Vectracor, Inc.

- Location (FDA's records): Totowa, NJ
- FDA decisions: 3 (2011–2018): 3 510(k) clearances
- Product codes: DPS (2), MSX (1)
- Predicates its devices cite: 7 (1 its own); citations of its devices by later devices: 2 (1 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
- Micromedical Industries, Ltd.: 2 (https://510kreport.com/company/micromedical-industries)
- Qrs Diagnostic, LLC: 1 (https://510kreport.com/company/qrs-diagnostic)
- Philips Medical Systems, Inc.: 1 (https://510kreport.com/company/philips-medical-systems)
- Datex-Ohmeda, Inc.: 1 (https://510kreport.com/company/datex-ohmeda)
- Shenzhen Mindray Bio-Medical Electronics Co., Ltd.: 1 (https://510kreport.com/company/shenzhen-mindray-bio-medical-electronics)

## Firms that cite its devices most
- AliveCor, Inc.: 1 (https://510kreport.com/company/alivecor)

## Its most-cited devices
- K102378: Vectraplexecg System with Vectraplexami (2011), cited by 1
- K173952: Universal SmartECG (2018), cited by 1

## Recent decisions
- K173952: Universal SmartECG (Aug 28, 2018)
- K140852: Vectraplex CMS (Jan 30, 2015)
- K102378: Vectraplexecg System with Vectraplexami (Nov 2, 2011)

Source page: https://510kreport.com/company/vectracor