# Revivant Corp.

- Location (FDA's records): Sunnyvale, CA
- FDA decisions: 4 (2001–2004): 4 510(k) clearances
- Product codes: DRM (4)
- Predicates its devices cite: 9 (6 its own); citations of its devices by later devices: 13 (6 its own)
- Recalls linked to its devices: 2 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Michigan Instruments, Inc.: 3 (https://510kreport.com/company/michigan-instruments)

## Firms that cite its devices most
- Zoll Circulation, Inc.: 5 (https://510kreport.com/company/zoll-circulation)
- Jolife AB: 2 (https://510kreport.com/company/jolife)

## Its most-cited devices
- K040453: Autopulse Resuscitation System, Model 100 (2004), cited by 4
- K011046: Autopulse, Model 100 (2001), cited by 4
- K022345: Autopulse Resuscitation System (2002), cited by 3
- K032852: Modification to: Autopulse Resuscitation System Model 100 (2003), cited by 2

## Recent decisions
- K040453: Autopulse Resuscitation System, Model 100 (Mar 11, 2004)
- K032852: Modification to: Autopulse Resuscitation System Model 100 (Nov 12, 2003)
- K022345: Autopulse Resuscitation System (Aug 15, 2002)
- K011046: Autopulse, Model 100 (Oct 25, 2001)

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