# Zmi Corp.

- Location (FDA's records): Woburn, MA
- FDA decisions: 8 (1986–1992): 8 510(k) clearances
- Product codes: DRO (4), LDD (2), LIH (1), DRF (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 3 (0 its own)
- Recalls linked to its devices: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Bio-Detek, Inc.: 1 (https://510kreport.com/company/bio-detek)
- ZOLL Medical Corporation: 1 (https://510kreport.com/company/zoll-medical)
- Anybattery, Inc.: 1 (https://510kreport.com/company/anybattery)

## Its most-cited devices
- K915159: Pediatric Multi-Function Electrodes (1992), cited by 2
- K913484: Zoll D-900 Defibrillator (1991), cited by 1

## Recent decisions
- K915100: Brindley & Smith ET-1000 (Sep 14, 1992)
- K915159: Pediatric Multi-Function Electrodes (Feb 7, 1992)
- K913484: Zoll D-900 Defibrillator (Dec 16, 1991)
- K911956: Zoll PD-1400 Pacer/Defibrillator (Jul 31, 1991)
- K895032: Zoll PD 2200 Pacing-Defibrillation Electrodes (Oct 12, 1989)
- K885166: Zmi Part NO. NTP-2100, Pediatric Electrodes (May 1, 1989)
- K873402: Zoll NTP-1200 Pacer/Defibrillator (Nov 23, 1987)
- K855015: Noninvasive Temp. Pacemaker NTP-1000 (Mar 31, 1986)

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