# Zoll Manufacturing Corporation

- Location (FDA's records): Pittsburgh, PA
- FDA decisions: 4 (2001–2019): 3 510(k) clearances and 1 original PMA approval
- Product codes: MHX (2), DPS (1), MVK (1)
- 510(k) review time since 2016: median 253 days, against 203 for FDA's reviews in the same codes and years (0 of 3 faster)
- Predicates its devices cite: 4 (1 its own); citations of its devices by later devices: 1 (1 its own)
- Recalls linked to its devices: 6 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Monebo Technologies, Inc.: 1 (https://510kreport.com/company/monebo-technologies)
- Corventis, Inc.: 1 (https://510kreport.com/company/corventis)
- Noninvasive Medical Technologies, Inc.: 1 (https://510kreport.com/company/noninvasive-medical-technologies)

## Its most-cited devices
- K172510: µCor Heart Failure and Arrhythmia Management System (2018), cited by 1

## Recent decisions
- K190939: ZOLL Arrhythmia Management Sysyem (Dec 19, 2019)
- K182093: ZOLL ECG Analysis Software (Jan 28, 2019)
- K172510: µCor Heart Failure and Arrhythmia Management System (May 11, 2018)
- P010030: Wearable Cardioverter Defibrillator (WCD) 2000 Lifevest (Dec 18, 2001)

Source page: https://510kreport.com/company/zoll-manufacturing